Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894040
rs104894040
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
G 0.700 CausalMutation CLINVAR
dbSNP: rs104894040
rs104894040
Entrez Id: 6469
Gene Symbol: SHH
SHH
CUI: C0079541
Disease:
Holoprosencephaly
C 0.700 CausalMutation CLINVAR