rs1554698613, PTCH1

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Basal Cell Nevus Syndrome
CUI: C0004779
Disease: Basal Cell Nevus Syndrome
124 1.000 0.160 9 95477680 splice acceptor variant TTAGACAGGCATAGGCGAGCTGCAAGCAGAACAATGG/- delins 0.700 1.000 2 2006 2006