Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs183211
rs183211
Entrez Id: 4905;474170
Gene Symbol: NSF;LRRC37A2
NSF;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease
0.800 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
dbSNP: rs183211
rs183211
Entrez Id: 4905;474170
Gene Symbol: NSF;LRRC37A2
NSF;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease
0.800 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
dbSNP: rs183211
rs183211
Entrez Id: 4905;474170
Gene Symbol: NSF;LRRC37A2
NSF;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease
0.800 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575 2009
dbSNP: rs199515
rs199515
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease
0.800 GeneticVariation GWASDB Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204 2012
dbSNP: rs199515
rs199515
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease
0.800 GeneticVariation GWASCAT Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204 2012
dbSNP: rs199533
rs199533
Entrez Id: 4905;474170
Gene Symbol: NSF;LRRC37A2
NSF;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease
0.800 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
dbSNP: rs199533
rs199533
Entrez Id: 4905;474170
Gene Symbol: NSF;LRRC37A2
NSF;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease
0.800 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
dbSNP: rs2074404
rs2074404
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0007570
Disease:
Celiac Disease
0.800 GeneticVariation GWASDB Multiple common variants for celiac disease influencing immune gene expression. 20190752 2010
dbSNP: rs2074404
rs2074404
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0007570
Disease:
Celiac Disease
0.800 GeneticVariation GWASCAT Multiple common variants for celiac disease influencing immune gene expression. 20190752 2010
dbSNP: rs387906881
rs387906881
Entrez Id: 9570;474170
Gene Symbol: GOSR2;LRRC37A2
GOSR2;LRRC37A2
CUI: C3279627
Disease:
EPILEPSY, PROGRESSIVE MYOCLONIC, 6
0.800 GeneticVariation UNIPROT A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia. 21549339 2011
dbSNP: rs415430
rs415430
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease
0.800 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
dbSNP: rs10853087
rs10853087
Entrez Id: 9570;474170
Gene Symbol: GOSR2;LRRC37A2
GOSR2;LRRC37A2
CUI: C0005845
Disease:
Blood urea nitrogen measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs11658276
rs11658276
Entrez Id: 474170
Gene Symbol: LRRC37A2
LRRC37A2
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs141899337
rs141899337
Entrez Id: 7484;474170
Gene Symbol: WNT9B;LRRC37A2
WNT9B;LRRC37A2
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs142167
rs142167
Entrez Id: 4905;474170
Gene Symbol: NSF;LRRC37A2
NSF;LRRC37A2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs144216645
rs144216645
Entrez Id: 51326;474170;100506084
Gene Symbol: ARL17A;LRRC37A2;ARL17B
ARL17A;LRRC37A2;ARL17B
CUI: C0023114
Disease:
Handedness
0.700 GeneticVariation GWASCAT The molecular genetics of hand preference revisited. 30980028 2019
dbSNP: rs169201
rs169201
Entrez Id: 4905;474170
Gene Symbol: NSF;LRRC37A2
NSF;LRRC37A2
CUI: C0206062
Disease:
Lung Diseases, Interstitial
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. 23583980 2013
dbSNP: rs169201
rs169201
Entrez Id: 4905;474170
Gene Symbol: NSF;LRRC37A2
NSF;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease
0.700 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
dbSNP: rs169201
rs169201
Entrez Id: 4905;474170
Gene Symbol: NSF;LRRC37A2
NSF;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
dbSNP: rs169201
rs169201
Entrez Id: 4905;474170
Gene Symbol: NSF;LRRC37A2
NSF;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease
0.700 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575 2009
dbSNP: rs17608766
rs17608766
Entrez Id: 9570;474170
Gene Symbol: GOSR2;LRRC37A2
GOSR2;LRRC37A2
CUI: C0871470
Disease:
Systolic Pressure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs17608766
rs17608766
Entrez Id: 9570;474170
Gene Symbol: GOSR2;LRRC37A2
GOSR2;LRRC37A2
CUI: C0007222
Disease:
Cardiovascular Diseases
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs17608766
rs17608766
Entrez Id: 9570;474170
Gene Symbol: GOSR2;LRRC37A2
GOSR2;LRRC37A2
CUI: C0429097
Disease:
QRS complex feature
0.700 GeneticVariation GWASCAT 52 Genetic Loci Influencing Myocardial Mass. 27659466 2016
dbSNP: rs183211
rs183211
Entrez Id: 4905;474170
Gene Symbol: NSF;LRRC37A2
NSF;LRRC37A2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs197920
rs197920
Entrez Id: 9570;474170
Gene Symbol: GOSR2;LRRC37A2
GOSR2;LRRC37A2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019