Variant: rs863224650 

    present in Gene: PTCH1;LOC100507346
    present in Chromosome: 9
    Position on Chromosome: 95469856
    Alleles of this Variant: G/A;T

rs863224650 in PTCH1;LOC100507346 gene and Neoplastic Syndromes, Hereditary PMID 16906569 2006 Patched mutations and hairy skin patches: a new sign in Gorlin syndrome.