RS113663584 PTCH1

Health Risk Chr 9:95449902 snv missense variant
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Associated Conditions
Hereditary cancer-predisposing syndrome
Gorlin syndrome
Holoprosencephaly 7
Gorlin syndrome
Hereditary cancer-predisposing syndrome
Gorlin syndrome
Holoprosencephaly 7
Gorlin syndrome
Population Frequencies
gnomAD ALL
0.1%
1kG AFR
100%
1kG ALL
100%
1kG AMR
99.9%
1kG EAS
100%
1kG EUR
99.9%
1kG SAS
100%
Other Variants in PTCH1
rs2117956624 rs199476090 rs2118419579 rs2118365442 rs2118041703 rs2136689212 rs587776689 rs138911275 rs199476093 rs2118336503
Ask Dr. Hemsworth about this variant