WNT7B, Wnt family member 7B, 7477

N. diseases: 53; N. variants: 5
Disease: ANOPHTHALMIA AND PULMONARY HYPOPLASIA ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1569119395
rs1569119395
Entrez Id: 7477
Gene Symbol: WNT7B
WNT7B
CUI: C1832661
Disease:
ANOPHTHALMIA AND PULMONARY HYPOPLASIA 		A 0.700 CausalMutation CLINVAR