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: 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: 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: rs1553132
rs1553132
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0424574
Disease:
Duration of sleep 		G 0.700 GeneticVariation GWASCAT Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways. 30804565 2019
dbSNP: rs1553132
rs1553132
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0424574
Disease:
Duration of sleep 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. 30846698 2019
dbSNP: rs7932640
rs7932640
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1269683
Disease:
Major Depressive Disorder 		T 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions. 30718901 2019
dbSNP: rs10501696
rs10501696
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1269683
Disease:
Major Depressive Disorder 		G 0.700 GeneticVariation GWASCAT Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways. 29662059 2018
dbSNP: rs11020496
rs11020496
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs11020496
rs11020496
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs1150313
rs1150313
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1269683
Disease:
Major Depressive Disorder 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs12792431
rs12792431
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0406208
Disease:
Suntan 		C 0.700 GeneticVariation GWASCAT Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. 29739929 2018
dbSNP: rs148065054
rs148065054
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0018498
Disease:
Hair Color 		T 0.700 GeneticVariation GWASCAT Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. 30531825 2018
dbSNP: rs34749698
rs34749698
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0406208
Disease:
Suntan 		C 0.700 GeneticVariation GWASCAT Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. 29739929 2018
dbSNP: rs4121827
rs4121827
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0406208
Disease:
Suntan 		C 0.700 GeneticVariation GWASCAT Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. 29739929 2018
dbSNP: rs6483414
rs6483414
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C1269683
Disease:
Major Depressive Disorder 		C 0.700 GeneticVariation GWASCAT Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways. 29662059 2018
dbSNP: rs71469216
rs71469216
Entrez Id: 2915
Gene Symbol: GRM5
GRM5
CUI: C0406208
Disease:
Suntan 		C 0.700 GeneticVariation GWASCAT Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. 29739929 2018
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