Gene: PTCH1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs781768965
rs781768965
PTCH1
A 0.700 CausalMutation CLINVAR Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome. 9096761

1997