RS368869806 PTCH1

Health Risk Chr 9:95485875
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What This Variant Does
"CLNSIG=4
Associated Conditions
Gorlin syndrome
Hereditary cancer-predisposing syndrome
Basal cell carcinoma
susceptibility to
1
PTCH1-related disorder
Holoprosencephaly 7
Basal cell nevus syndrome 1
Gorlin syndrome
Hereditary cancer-predisposing syndrome
Basal cell carcinoma
susceptibility to
1
PTCH1-related disorder
Holoprosencephaly 7
Other Variants in PTCH1
rs2117956624 rs199476090 rs2118419579 rs2118365442 rs2118041703 rs2136689212 rs587776689 rs138911275 rs199476093 rs2118336503
Ask Dr. Hemsworth about this variant