WNT6, Wnt family member 6, 7475

N. diseases: 35; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs544577047
rs544577047
Entrez Id: 7475
Gene Symbol: WNT6
WNT6
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs7558440
rs7558440
Entrez Id: 7475
Gene Symbol: WNT6
WNT6
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10193725
rs10193725
Entrez Id: 7475
Gene Symbol: WNT6
WNT6
CUI: C0002170
Disease:
Alopecia 		C 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs6747776
rs6747776
Entrez Id: 7475
Gene Symbol: WNT6
WNT6
CUI: C1302401
Disease:
Adenoma of large intestine 		0.010 GeneticVariation BEFREE The WNT6 rs6747776 homozygous minor allele (CC) was associated with increased risk of colorectal adenoma (OR = 2.75, 95% CI: 1.03-7.31). 21547848 2011