rs746339472, PTCH1

N. diseases: 2
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.
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 1.000 0.040 9 95506413 missense variant C/T snv 8.0E-06 2.1E-05 0.010 1.000 1 2016 2016
Experimental Organism Basal Cell Carcinoma
63 1.000 0.040 9 95506413 missense variant C/T snv 8.0E-06 2.1E-05 0.010 1.000 1 2016 2016