RS1360279030 PTCH1

Health Risk Chr 9:95506526
Upload your DNA to see your genotype for this variant.
Associated Conditions
Hereditary cancer-predisposing syndrome
Gorlin syndrome
Basal cell carcinoma
susceptibility to
1
Basal cell nevus syndrome 1
Holoprosencephaly 7
Hereditary cancer-predisposing syndrome
Gorlin syndrome
Hereditary cancer-predisposing syndrome
Gorlin syndrome
Basal cell carcinoma
susceptibility to
1
Basal cell nevus syndrome 1
Other Variants in PTCH1
rs2117956624 rs199476090 rs2118419579 rs2118365442 rs2118041703 rs2136689212 rs587776689 rs138911275 rs199476093 rs2118336503
Ask Dr. Hemsworth about this variant