GPC5, glypican 5, 2262

N. diseases: 2; N. variants: 14
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9523762
rs9523762
Entrez Id: 2262;105370315
Gene Symbol: GPC5;LOC105370315
GPC5;LOC105370315
CUI: C0026769
Disease:
Multiple Sclerosis 		0.820 GeneticVariation GWASDB Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. 19010793 2009
dbSNP: rs9523762
rs9523762
Entrez Id: 2262;105370315
Gene Symbol: GPC5;LOC105370315
GPC5;LOC105370315
CUI: C0026769
Disease:
Multiple Sclerosis 		0.820 GeneticVariation GWASCAT Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. 19010793 2009
dbSNP: rs7982677
rs7982677
Entrez Id: 2262
Gene Symbol: GPC5
GPC5
CUI: C0039685
Disease:
Tetralogy of Fallot 		A 0.800 GeneticVariation GWASCAT Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. 23297363 2013
dbSNP: rs7982677
rs7982677
Entrez Id: 2262
Gene Symbol: GPC5
GPC5
CUI: C0039685
Disease:
Tetralogy of Fallot 		A 0.800 GeneticVariation GWASDB Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. 23297363 2013
dbSNP: rs138994828
rs138994828
Entrez Id: 2262
Gene Symbol: GPC5
GPC5
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936. 31320639 2019
dbSNP: rs1929922
rs1929922
Entrez Id: 2262
Gene Symbol: GPC5
GPC5
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936. 31320639 2019
dbSNP: rs9516053
rs9516053
Entrez Id: 2262
Gene Symbol: GPC5
GPC5
CUI: C0003873
Disease:
Rheumatoid Arthritis 		C 0.700 GeneticVariation GWASCAT Genetic influences on susceptibility to rheumatoid arthritis in African-Americans. 30423114 2019
dbSNP: rs342702
rs342702
Entrez Id: 2262
Gene Symbol: GPC5
GPC5
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs342702
rs342702
Entrez Id: 2262
Gene Symbol: GPC5
GPC5
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs4643170
rs4643170
Entrez Id: 2262;100873969
Gene Symbol: GPC5;GPC5-AS1
GPC5;GPC5-AS1
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs4771856
rs4771856
Entrez Id: 2262;100873970
Gene Symbol: GPC5;GPC5-AS2
GPC5;GPC5-AS2
CUI: C0039685
Disease:
Tetralogy of Fallot 		0.700 GeneticVariation GWASDB Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. 23297363 2013
dbSNP: rs4771859
rs4771859
Entrez Id: 2262
Gene Symbol: GPC5
GPC5
CUI: C3548510
Disease:
response to antineoplastic agent 		G 0.700 GeneticVariation GWASCAT Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. 23648065 2013
dbSNP: rs7328464
rs7328464
Entrez Id: 2262
Gene Symbol: GPC5
GPC5
CUI: C0162701
Disease:
Polysomnography 		A 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs7981515
rs7981515
Entrez Id: 2262
Gene Symbol: GPC5
GPC5
CUI: C0162701
Disease:
Polysomnography 		0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs16946160
rs16946160
Entrez Id: 2262
Gene Symbol: GPC5
GPC5
CUI: C0027726
Disease:
Nephrotic Syndrome 		A 0.700 GeneticVariation GWASCAT Common variation in GPC5 is associated with acquired nephrotic syndrome. 21441931 2011
dbSNP: rs1411741
rs1411741
Entrez Id: 2262
Gene Symbol: GPC5
GPC5
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
dbSNP: rs17267292
rs17267292
Entrez Id: 2262;105370315
Gene Symbol: GPC5;LOC105370315
GPC5;LOC105370315
CUI: C0523744
Disease:
Lipids measurement 		0.700 GeneticVariation GWASCAT Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. 19043545 2008
dbSNP: rs17267292
rs17267292
Entrez Id: 2262;105370315
Gene Symbol: GPC5;LOC105370315
GPC5;LOC105370315
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. 19043545 2008