WNT10B, Wnt family member 10B, 7480

N. diseases: 90; N. variants: 23
Disease: OSTEOGENESIS IMPERFECTA, TYPE XV ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907356
rs387907356
Entrez Id: 7471;7480
Gene Symbol: WNT1;WNT10B
WNT1;WNT10B
CUI: C3808844
Disease:
OSTEOGENESIS IMPERFECTA, TYPE XV 		A 0.700 CausalMutation CLINVAR