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: rs3802842
rs3802842
0.695 0.280 11 111300984 intron variant C/A snv 0.71
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 8 2008 2019
dbSNP: rs6589219
rs6589219
0.790 0.080 11 111302186 intron variant G/C snv 0.69
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2018 2018