RS149133805 PTCH2

Health Risk Chr 1:44827037
Upload your DNA to see your genotype for this variant.
Associated Conditions
Gorlin syndrome
Basal cell carcinoma
susceptibility to
1
Medulloblastoma
Gorlin syndrome
Basal cell carcinoma
susceptibility to
1
Medulloblastoma
Other Variants in PTCH2
rs2148874807 rs375844056 rs200216295 rs201345708 rs200355030 rs199959462 rs752886480 rs560010627 rs2521979430 rs771498368
Ask Dr. Hemsworth about this variant