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: rs1741640
rs1741640
0.776 0.080 20 62357358 intron variant T/C snv 0.66
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 2 2019 2019
dbSNP: rs4925386
rs4925386
0.776 0.080 20 62345988 intron variant T/C snv 0.56
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2010 2010