RS138911275 PTCH1

Health Risk Chr 9:95458026
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What This Variant Does
"CLNSIG=5
Associated Conditions
Holoprosencephaly 7
Holoprosencephaly sequence
Hereditary cancer-predisposing syndrome
Gorlin syndrome
PTCH1-related disorder
Holoprosencephaly 7
Holoprosencephaly sequence
Hereditary cancer-predisposing syndrome
Gorlin syndrome
PTCH1-related disorder
Other Variants in PTCH1
rs2117956624 rs199476090 rs2118419579 rs2118365442 rs2118041703 rs2136689212 rs587776689 rs199476093 rs2118336503 rs1587692888
Ask Dr. Hemsworth about this variant