SERPINH1, serpin family H member 1, 871

N. diseases: 148; N. variants: 8
Disease: OSTEOGENESIS IMPERFECTA, TYPE X ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886039819
rs886039819
Entrez Id: 871
Gene Symbol: SERPINH1
SERPINH1
CUI: C3151211
Disease:
OSTEOGENESIS IMPERFECTA, TYPE X 		C 0.700 CausalMutation CLINVAR