RS80168454 PTCH2

Health Risk Chr 1:44832296
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
rs546170078 rs200216295 rs201345708 rs200355030 rs199959462 rs752886480 rs2148874807 rs771498368 rs149133805 rs2521979430
Ask Dr. Hemsworth about this variant