RS138588008 PTCH2
Upload your DNA to see your genotype for this variant.
Associated Conditions
Gorlin syndrome
Basal cell carcinoma
susceptibility to
1
Medulloblastoma
PTCH2-related disorder
Gorlin syndrome
Basal cell carcinoma
susceptibility to
1
Medulloblastoma
PTCH2-related disorder
Other Variants in PTCH2