GRM5, glutamate metabotropic receptor 5, 2915

N. diseases: 189; N. variants: 37
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1353804
rs1353804
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs1353806
rs1353806
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs1391874
rs1391874
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs1499032
rs1499032
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs1499035
rs1499035
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs16914552
rs16914552
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs16915130
rs16915130
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs1846442
rs1846442
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs1846443
rs1846443
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs1846444
rs1846444
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs6483380
rs6483380
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs6483387
rs6483387
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs7479186
rs7479186
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs7480724
rs7480724
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs904463
rs904463
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs655683
rs655683
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0025303
Disease:
Meningococcal Infections 		0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
dbSNP: rs10501678
rs10501678
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs10501678
rs10501678
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs10501678
rs10501678
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs10501678
rs10501678
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs10831496
rs10831496
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0406208
Disease:
Suntan 		G 0.700 GeneticVariation GWASCAT Genome-wide association study of tanning phenotype in a population of European ancestry. 19340012 2009
dbSNP: rs12273907
rs12273907
Entrez Id: 2915;100873989
Gene Symbol: GRM5;GRM5-AS1
GRM5;GRM5-AS1
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
dbSNP: rs3824927
rs3824927
Entrez Id: 2915;100873989
Gene Symbol: GRM5;GRM5-AS1
GRM5;GRM5-AS1
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE For rs3824927, compared to major allele homozygotes, minor allele carriers with schizophrenia had lower Intelligence Quotients (IQ). 28405888 2018
dbSNP: rs60954128
rs60954128
Entrez Id: 2915;100873989
Gene Symbol: GRM5;GRM5-AS1
GRM5;GRM5-AS1
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE Schizophrenia minor allele carriers of rs60954128 had reduced right hippocampal volume relative to healthy controls of the same genotype (-12.3%); this effect was exaggerated in males with schizophrenia (-15.6%). 28405888 2018
dbSNP: rs7102764
rs7102764
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0279702
Disease:
Conventional (Clear Cell) Renal Cell Carcinoma 		0.010 GeneticVariation BEFREE After adjustment for known risk factors, GRM5 rs7102764 T was associated with an increased risk of RCC (P = 0.006). 30488581 2018