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: rs12594720
rs12594720
0.776 0.080 15 66714680 intron variant C/G snv 0.23
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019
dbSNP: rs4776316
rs4776316
0.790 0.080 15 66715475 intron variant A/G snv 0.26
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019