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: rs12241008
rs12241008
0.716 0.160 10 112520943 intron variant T/C snv 0.13
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 3 2014 2019
dbSNP: rs10506868
rs10506868
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2016 2016
dbSNP: rs12246635
rs12246635
0.776 0.080 10 112528860 intron variant T/C snv 0.13
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019
dbSNP: rs12255141
rs12255141
0.790 0.080 10 112535133 intron variant A/G;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019