Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2228527
rs2228527
0.925 0.080 10 49470323 missense variant T/C snv 0.22 0.20
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell
Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs2228529
rs2228529
0.925 0.080 10 49459059 missense variant T/C snv 0.22 0.19
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell
Neoplasms 0.010 1.000 1 2012 2012