RARRES2, retinoic acid receptor responder 2, 5919

N. diseases: 180; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3735167
rs3735167
Entrez Id: 5919;107986858
Gene Symbol: RARRES2;LOC107986858
RARRES2;LOC107986858
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs17173608
rs17173608
Entrez Id: 5919
Gene Symbol: RARRES2
RARRES2
CUI: C0038663
Disease:
Suicide attempt
G 0.700 GeneticVariation GWASCAT Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. 24964207 2014
dbSNP: rs17173608
rs17173608
Entrez Id: 5919
Gene Symbol: RARRES2
RARRES2
CUI: C1269683
Disease:
Major Depressive Disorder
G 0.700 GeneticVariation GWASCAT Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. 24964207 2014
dbSNP: rs17173608
rs17173608
Entrez Id: 5919
Gene Symbol: RARRES2
RARRES2
CUI: C0005586
Disease:
Bipolar Disorder
G 0.700 GeneticVariation GWASCAT Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. 24964207 2014
dbSNP: rs17173608
rs17173608
Entrez Id: 5919
Gene Symbol: RARRES2
RARRES2
CUI: C0524620
Disease:
Metabolic Syndrome X
0.020 GeneticVariation BEFREE Metabolic syndrome in Egyptian females is associated with the minor allele of chemerin rs17173608 polymorphism, whereas the minor allele of vaspin rs2236242 polymorphism plays a protective role against metabolic syndrome. 26472663 2016
dbSNP: rs17173608
rs17173608
Entrez Id: 5919
Gene Symbol: RARRES2
RARRES2
CUI: C0524620
Disease:
Metabolic Syndrome X
0.020 GeneticVariation BEFREE In conclusion, our data suggest for the first time a significant association between vaspin rs2236242 and chemerin rs17173608 polymorphisms and the MeS in Zahedan, southeast Iran. 22982016 2012
dbSNP: rs3735167
rs3735167
Entrez Id: 5919;107986858
Gene Symbol: RARRES2;LOC107986858
RARRES2;LOC107986858
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE Chemerin levels, but not the rs3735167 genotypes, predicted the long-term outcome of CAD, especially when combined with CRP levels. 30866520 2019
dbSNP: rs10278590
rs10278590
Entrez Id: 5919;65999
Gene Symbol: RARRES2;LRRC61
RARRES2;LRRC61
CUI: C0085207
Disease:
Gestational Diabetes
0.010 GeneticVariation BEFREE This case-control study was designed to assess the relation between chemerin SNPs rs4721 (or rs10278590) and rs17173608 and the development of GDM. 29360607 2018
dbSNP: rs17173608
rs17173608
Entrez Id: 5919
Gene Symbol: RARRES2
RARRES2
CUI: C0085207
Disease:
Gestational Diabetes
0.010 GeneticVariation BEFREE Moreover, the genotypes and allele frequencies of chemerin rs17173608 polymorphism did not show significant differences between GDM and non-GDM (P > 0.05). 29360607 2018
dbSNP: rs17173608
rs17173608
Entrez Id: 5919
Gene Symbol: RARRES2
RARRES2
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.010 GeneticVariation BEFREE We found that the G allele of chemerin rs17173608 compared to T allele decreased the risk of ESRD, and there was a significant association between chemerin and vaspin variants with plasma MDA level in a sample of the Iranian population. 29644922 2018
dbSNP: rs17173608
rs17173608
Entrez Id: 5919
Gene Symbol: RARRES2
RARRES2
CUI: C2316810
Disease:
Chronic kidney disease stage 5
0.010 GeneticVariation BEFREE We found that the G allele of chemerin rs17173608 compared to T allele decreased the risk of ESRD, and there was a significant association between chemerin and vaspin variants with plasma MDA level in a sample of the Iranian population. 29644922 2018
dbSNP: rs4721
rs4721
Entrez Id: 5919;65999
Gene Symbol: RARRES2;LRRC61
RARRES2;LRRC61
CUI: C0085207
Disease:
Gestational Diabetes
0.010 GeneticVariation BEFREE The genotype of rs4721 was significantly associated with GDM in co-dominant and dominant genotypes (GG vs GT, OR = 2.3, 95%CI = 1.24-4.24, P = 0.008, and GG vs GT + TT, OR = 2.21, 95%CI = 1.23-3.99, P = 0.008, respectively). 29360607 2018
dbSNP: rs4721
rs4721
Entrez Id: 5919;65999
Gene Symbol: RARRES2;LRRC61
RARRES2;LRRC61
CUI: C0029408
Disease:
Degenerative polyarthritis
0.010 GeneticVariation BEFREE The minor allele of RETN rs10401670 was associated with a decreased [odds ratio (OR) = 0.73, 95% confidence interval (CI) 0.55-0.97, p = 0.03] and RARRES2 rs4721 with an increased (OR 1.41, 95% CI 1.07-1.87, p = 0.01) prevalence of hand OA. 28812414 2018
dbSNP: rs17173608
rs17173608
Entrez Id: 5919
Gene Symbol: RARRES2
RARRES2
CUI: C0032460
Disease:
Polycystic Ovary Syndrome
0.010 GeneticVariation BEFREE Influence of chemerin rs17173608 polymorphism on polycystic ovary syndrome susceptibility. 26166341 2015