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: rs121918347
rs121918347
0.851 0.080 7 129210500 missense variant G/T snv
CUI: C3838465
Disease: BASAL CELL CARCINOMA, SOMATIC
BASAL CELL CARCINOMA, SOMATIC
0.700 0
dbSNP: rs121918348
rs121918348
0.925 0.040 7 129210997 missense variant G/A snv 4.0E-05 2.8E-05
CUI: C3838465
Disease: BASAL CELL CARCINOMA, SOMATIC
BASAL CELL CARCINOMA, SOMATIC
0.700 0