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: 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: rs16914280
rs16914280
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs16914280
rs16914280
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs16914280
rs16914280
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.800 GeneticVariation GWASCAT Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs16914280
rs16914280
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		0.800 GeneticVariation GWASCAT Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs16914280
rs16914280
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs16914280
rs16914280
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 GeneticVariation GWASCAT Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs16914280
rs16914280
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		0.800 GeneticVariation GWASCAT Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs16914280
rs16914280
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 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: 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: 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: rs5016282
rs5016282
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		A 0.800 GeneticVariation GWASDB Genome-wide association study in German patients with attention deficit/hyperactivity disorder. 22012869 2011
dbSNP: rs5016282
rs5016282
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		A 0.800 GeneticVariation GWASCAT Genome-wide association study in German patients with attention deficit/hyperactivity disorder. 22012869 2011
dbSNP: rs10741500
rs10741500
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: rs1353802
rs1353802
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: 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