WNT3, Wnt family member 3, 7473

N. diseases: 140; N. variants: 22
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199498
rs199498
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease 		T 0.800 GeneticVariation GWASCAT Identification of a novel Parkinson's disease locus via stratified genome-wide association study. 24511991 2014
dbSNP: rs199498
rs199498
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease 		T 0.800 GeneticVariation GWASDB Identification of a novel Parkinson's disease locus via stratified genome-wide association study. 24511991 2014
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: 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: rs415430
rs415430
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease 		T 0.800 GeneticVariation GWASDB Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. 21812969 2011
dbSNP: rs415430
rs415430
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0030567
Disease:
Parkinson Disease 		T 0.800 GeneticVariation GWASCAT Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. 21812969 2011
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: rs199512
rs199512
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0023114
Disease:
Handedness 		C 0.700 GeneticVariation GWASCAT In particular, with rs199512, we identified a common genetic influence on handedness, psychiatric phenotypes, Parkinson's disease, and the integrity of white matter tracts connecting the same language-related regions identified in the handedness-imaging analysis. 31504236 2019
dbSNP: rs916888
rs916888
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs1563304
rs1563304
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0004238
Disease:
Atrial Fibrillation 		T 0.700 GeneticVariation GWASCAT Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. 30061737 2018
dbSNP: rs199505
rs199505
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C1269683
Disease:
Major Depressive Disorder 		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: rs199505
rs199505
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0525045
Disease:
Mood Disorders 		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: rs199525
rs199525
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0016529
Disease:
Forced expiratory volume function 		T 0.700 GeneticVariation GWASCAT Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. 30061609 2018
dbSNP: rs199525
rs199525
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0042834
Disease:
Vital capacity 		T 0.700 GeneticVariation GWASCAT Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. 30061609 2018
dbSNP: rs2074404
rs2074404
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs916888
rs916888
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0016529
Disease:
Forced expiratory volume function 		T 0.700 GeneticVariation GWASCAT Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. 30061609 2018
dbSNP: rs916888
rs916888
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. 30061609 2018
dbSNP: rs199498
rs199498
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0678222
Disease:
Breast Carcinoma 		C 0.700 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683 2017
dbSNP: rs916888
rs916888
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium. 28093568 2017
dbSNP: rs8069437
rs8069437
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0018935
Disease:
Hematocrit procedure 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs8069437
rs8069437
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0518015
Disease:
Hemoglobin measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs8069437
rs8069437
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs415430
rs415430
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0206062
Disease:
Lung Diseases, Interstitial 		0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. 23583980 2013