Variant: rs878853852 

    present in Gene: PTCH1;LOC100507346
    present in Chromosome: 9
    Position on Chromosome: 95462000
    Alleles of this Variant: T/A;C

rs878853852 in PTCH1;LOC100507346 gene and Basal Cell Nevus Syndrome PMID 16419085 2006 PTCH mutations: distribution and analyses.

PMID 16301862 2006 Clinical testing for the nevoid basal cell carcinoma syndrome in a DNA diagnostic laboratory.