Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17689918
rs17689918
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0338908
Disease:
Mixed anxiety and depressive disorder
0.010 GeneticVariation BEFREE We assess the effects of CRHR1 variant (rs17689918)-by-environment interactions on emotionality and behavioral traits, including anxiety, depression, aggression and antisocial behaviors. 29772307 2018
dbSNP: rs242948
rs242948
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C3887898
Disease:
Infantile Spasm
0.010 GeneticVariation BEFREE Under the assumption of the dominant model, the selected five SNPs, rs4458044, rs171440, rs17689966, rs28364026 and rs242948, showed no association with the risk of infantile spasms and the effectiveness of adrenocorticotropic hormone treatment. 25954915 2015
dbSNP: rs242948
rs242948
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0037769
Disease:
West Syndrome
0.010 GeneticVariation BEFREE Under the assumption of the dominant model, the selected five SNPs, rs4458044, rs171440, rs17689966, rs28364026 and rs242948, showed no association with the risk of infantile spasms and the effectiveness of adrenocorticotropic hormone treatment. 25954915 2015
dbSNP: rs242941
rs242941
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C1269683
Disease:
Major Depressive Disorder
0.030 GeneticVariation BEFREE To investigate the possible relationship between genetic risk factors and depression in AD, we assessed genetic polymorphisms reported to be associated with depression (MAOA VNTR, ACE 288bp Insertion/ Deletion, 5HTTLPR, COMT Val158Met, BDNF Val66Met, TPH1 A218C, HTR2A T102C, P2RX7 Q460R, FKBP5 rs1360780 and CRHR1 rs242941) in a cross-sectional study on 246 AD patients with or without clinically significant major depressive disorder (MDD) according to DSM-IV. 23157339 2013
dbSNP: rs242941
rs242941
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE To investigate the possible relationship between genetic risk factors and depression in AD, we assessed genetic polymorphisms reported to be associated with depression (MAOA VNTR, ACE 288bp Insertion/ Deletion, 5HTTLPR, COMT Val158Met, BDNF Val66Met, TPH1 A218C, HTR2A T102C, P2RX7 Q460R, FKBP5 rs1360780 and CRHR1 rs242941) in a cross-sectional study on 246 AD patients with or without clinically significant major depressive disorder (MDD) according to DSM-IV. 23157339 2013
dbSNP: rs242941
rs242941
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0011581
Disease:
Depressive disorder
0.030 GeneticVariation BEFREE To investigate the possible relationship between genetic risk factors and depression in AD, we assessed genetic polymorphisms reported to be associated with depression (MAOA VNTR, ACE 288bp Insertion/ Deletion, 5HTTLPR, COMT Val158Met, BDNF Val66Met, TPH1 A218C, HTR2A T102C, P2RX7 Q460R, FKBP5 rs1360780 and CRHR1 rs242941) in a cross-sectional study on 246 AD patients with or without clinically significant major depressive disorder (MDD) according to DSM-IV. 23157339 2013
dbSNP: rs242941
rs242941
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0344315
Disease:
Depressed mood
0.020 GeneticVariation BEFREE To investigate the possible relationship between genetic risk factors and depression in AD, we assessed genetic polymorphisms reported to be associated with depression (MAOA VNTR, ACE 288bp Insertion/ Deletion, 5HTTLPR, COMT Val158Met, BDNF Val66Met, TPH1 A218C, HTR2A T102C, P2RX7 Q460R, FKBP5 rs1360780 and CRHR1 rs242941) in a cross-sectional study on 246 AD patients with or without clinically significant major depressive disorder (MDD) according to DSM-IV. 23157339 2013
dbSNP: rs242941
rs242941
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0011570
Disease:
Mental Depression
0.020 GeneticVariation BEFREE To investigate the possible relationship between genetic risk factors and depression in AD, we assessed genetic polymorphisms reported to be associated with depression (MAOA VNTR, ACE 288bp Insertion/ Deletion, 5HTTLPR, COMT Val158Met, BDNF Val66Met, TPH1 A218C, HTR2A T102C, P2RX7 Q460R, FKBP5 rs1360780 and CRHR1 rs242941) in a cross-sectional study on 246 AD patients with or without clinically significant major depressive disorder (MDD) according to DSM-IV. 23157339 2013
dbSNP: rs1876831
rs1876831
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0086132
Disease:
Depressive Symptoms
0.010 GeneticVariation BEFREE To determine if single nucleotide polymorphisms of the corticotrophin-releasing hormone binding protein (CRHBP, rs10055255) and CRH receptor type 1 (CRHR1, rs1876831) were associated with posttraumatic stress disorder (PTSD) and depressive symptoms following medical-surgical intensive care unit (ICU) hospitalization. 24075295 2014
dbSNP: rs1876831
rs1876831
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0038436
Disease:
Post-Traumatic Stress Disorder
0.010 GeneticVariation BEFREE To determine if single nucleotide polymorphisms of the corticotrophin-releasing hormone binding protein (CRHBP, rs10055255) and CRH receptor type 1 (CRHR1, rs1876831) were associated with posttraumatic stress disorder (PTSD) and depressive symptoms following medical-surgical intensive care unit (ICU) hospitalization. 24075295 2014
dbSNP: rs173365
rs173365
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0030319
Disease:
Panic Disorder
0.010 GeneticVariation BEFREE To confirm the association of CRHR1 and CRHR2 with MDD and PD, we investigated 12 single nucleotide polymorphisms (SNPs) (rs4076452, rs7209436, rs110402, rs242924, rs242940, and rs173365 for CRHR1 and rs4722999, rs3779250, rs2267710, rs1076292, rs2284217, and rs226771 for CRHR2) in MDD patients (n = 173), PD patients (n = 180), and healthy controls (n = 285). 22467522 2012
dbSNP: rs4792887
rs4792887
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0344315
Disease:
Depressed mood
0.010 GeneticVariation BEFREE To comprehensively map the genetic variation in CRHR1 in relation to suicidality and depression, as a follow-up to our initial report on SNP rs4792887, we analyzed six new single nucleotide polymorphisms (SNPs), in an extended sample of family trios (n = 672) with suicide attempter offspring, by using family-based association tests. 19220485 2009
dbSNP: rs4792887
rs4792887
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0011570
Disease:
Mental Depression
0.010 GeneticVariation BEFREE To comprehensively map the genetic variation in CRHR1 in relation to suicidality and depression, as a follow-up to our initial report on SNP rs4792887, we analyzed six new single nucleotide polymorphisms (SNPs), in an extended sample of family trios (n = 672) with suicide attempter offspring, by using family-based association tests. 19220485 2009
dbSNP: rs4792887
rs4792887
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0011581
Disease:
Depressive disorder
0.010 GeneticVariation BEFREE To comprehensively map the genetic variation in CRHR1 in relation to suicidality and depression, as a follow-up to our initial report on SNP rs4792887, we analyzed six new single nucleotide polymorphisms (SNPs), in an extended sample of family trios (n = 672) with suicide attempter offspring, by using family-based association tests. 19220485 2009
dbSNP: rs12936511
rs12936511
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0011570
Disease:
Mental Depression
0.010 GeneticVariation BEFREE Thus, while the characteristics of the suicide female attempters remained undetermined, the male suicidal offspring had increased depression intensity related to main genetic effects by exonic SNP rs12936511 and homozygous non-CGC haplotypes. 19220485 2009
dbSNP: rs12936511
rs12936511
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0344315
Disease:
Depressed mood
0.010 GeneticVariation BEFREE Thus, while the characteristics of the suicide female attempters remained undetermined, the male suicidal offspring had increased depression intensity related to main genetic effects by exonic SNP rs12936511 and homozygous non-CGC haplotypes. 19220485 2009
dbSNP: rs12936511
rs12936511
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0011581
Disease:
Depressive disorder
0.010 GeneticVariation BEFREE Thus, while the characteristics of the suicide female attempters remained undetermined, the male suicidal offspring had increased depression intensity related to main genetic effects by exonic SNP rs12936511 and homozygous non-CGC haplotypes. 19220485 2009
dbSNP: rs242941
rs242941
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0347950
Disease:
Asthma attack
0.010 GeneticVariation BEFREE Thus, CRHR1 gene SNP rs242941 polymorphism is associated with better response to systemic corticosteroid during acute exacerbation of asthma. 25712009 2015
dbSNP: rs7209436
rs7209436
Entrez Id: 1394;104909134
Gene Symbol: CRHR1;LINC02210-CRHR1
CRHR1;LINC02210-CRHR1
CUI: C0022104
Disease:
Irritable Bowel Syndrome
0.030 GeneticVariation BEFREE Three CRH-R1 SNPS (rs110402, rs242924, and rs7209436) were genotyped using salivary DNA from IBS and healthy control subjects (HCs). 27497153 2016
dbSNP: rs110402
rs110402
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic
0.010 GeneticVariation BEFREE This study examined the influence of an intronic CRHR1 gene variant, rs110402, on brain responses to negative emotional words, negative emotional traits, and alcohol use in adolescents and young adults at high risk for alcoholism. 24623788 2014
dbSNP: rs110402
rs110402
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0008060
Disease:
child abuse behavior
0.030 GeneticVariation BEFREE This study examined the contributions of a polymorphism of the corticotropin-releasing hormone receptor type I (CRHR1) gene (rs110402) and a history of child maltreatment--alone and in interaction--to patterns of cortisol reactivity in adolescents. 24703172 2014
dbSNP: rs242941
rs242941
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C4284586
Disease:
Perinatal depression in mother
0.010 GeneticVariation BEFREE There was no statistically significant association of perinatal depression for CRHR1 rs242941 and GR rs41423247 (BclI). 26518448 2015
dbSNP: rs242924
rs242924
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C0022104
Disease:
Irritable Bowel Syndrome
0.020 GeneticVariation BEFREE The TT genotype of rs7209436 (P = 0.01) and rs242924 (P = 0.02) was significantly more common in patients with IBS than in controls. 22957021 2012
dbSNP: rs7209436
rs7209436
Entrez Id: 1394;104909134
Gene Symbol: CRHR1;LINC02210-CRHR1
CRHR1;LINC02210-CRHR1
CUI: C0022104
Disease:
Irritable Bowel Syndrome
0.030 GeneticVariation BEFREE The TT genotype of rs7209436 (P = 0.01) and rs242924 (P = 0.02) was significantly more common in patients with IBS than in controls. 22957021 2012
dbSNP: rs173365
rs173365
Entrez Id: 1394;100128977;104909134
Gene Symbol: CRHR1;MAPT-AS1;LINC02210-CRHR1
CRHR1;MAPT-AS1;LINC02210-CRHR1
CUI: C1269683
Disease:
Major Depressive Disorder
0.010 GeneticVariation BEFREE The T-A-T-G-G haplotype consisting of rs7209436 and rs173365 in CRHR1 was positively associated with MDD. 22467522 2012