RS1554698260 PTCH1

Health Risk Chr 9:95476782
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Associated Conditions
Inborn genetic diseases
Gorlin syndrome
Inborn genetic diseases
Gorlin syndrome
Other Variants in PTCH1
rs2117956624 rs199476090 rs2118419579 rs2118365442 rs2118041703 rs2136689212 rs587776689 rs138911275 rs199476093 rs2118336503
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