Gene: PTCH1 ×
Source: CLINVAR ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs147067171
rs147067171
PTCH1
2 0.925 0.080 9 95447309 missense variant T/C snv 5.5E-04 5.0E-04 0.700 1.000 1 2016 2016
dbSNP: rs765371196
rs765371196
PTCH1 ; LOC100507346
1 1.000 9 95461864 missense variant T/C snv 1.6E-05 1.4E-05 0.700 1.000 1 2016 2016