Disease: Opsismodysplasia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797044468
rs797044468
Entrez Id: 3636
Gene Symbol: INPPL1
INPPL1
CUI: C0432219
Disease:
Opsismodysplasia 		C 0.700 CausalMutation CLINVAR