RS1064794260 PTCH1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Gorlin syndrome
Hereditary cancer-predisposing syndrome
Gorlin syndrome
Hereditary cancer-predisposing syndrome
Gorlin syndrome
Hereditary cancer-predisposing syndrome
Gorlin syndrome
Other Variants in PTCH1