Gene: PTCH1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878853856
rs878853856
PTCH1
G 0.800 GeneticVariation CLINVAR

dbSNP: rs1057520590
rs1057520590
PTCH1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060502264
rs1060502264
PTCH1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060502271
rs1060502271
PTCH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502273
rs1060502273
PTCH1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060502274
rs1060502274
PTCH1 ; LOC100507346
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502277
rs1060502277
PTCH1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060502278
rs1060502278
PTCH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502280
rs1060502280
PTCH1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060502281
rs1060502281
PTCH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502285
rs1060502285
PTCH1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1060502286
rs1060502286
PTCH1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060502287
rs1060502287
PTCH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502294
rs1060502294
PTCH1 ; LOC100507346
TA 0.700 CausalMutation CLINVAR

dbSNP: rs1060502295
rs1060502295
PTCH1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060502297
rs1060502297
PTCH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502298
rs1060502298
PTCH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502301
rs1060502301
PTCH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1064793922
rs1064793922
PTCH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131690969
rs1131690969
PTCH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1333346461
rs1333346461
PTCH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1344258746
rs1344258746
PTCH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1356231878
rs1356231878
PTCH1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1432645175
rs1432645175
PTCH1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554689667
rs1554689667
PTCH1
GGA 0.700 CausalMutation CLINVAR