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: rs12427600
rs12427600
0.790 0.080 13 36886511 intron variant T/C snv 0.23
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2019 2019
dbSNP: rs7333607
rs7333607
0.776 0.080 13 36887873 intron variant A/G snv 0.24
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2019 2019