RS56126236 PTCH2

Health Risk Chr 1:44829444
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What This Variant Does
"CLNSIG=5
Associated Conditions
Medulloblastoma
Gorlin syndrome
Basal cell carcinoma
susceptibility to
1
Medulloblastoma
Gorlin syndrome
Basal cell carcinoma
susceptibility to
1
Other Variants in PTCH2
rs546170078 rs200216295 rs201345708 rs200355030 rs199959462 rs752886480 rs2148874807 rs771498368 rs149133805 rs2521979430
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