Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs16969681
rs16969681
0.776 0.080 15 32700910 downstream gene variant C/T snv 0.11
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 3 2019 2019
dbSNP: rs1800469
rs1800469
0.547 0.760 19 41354391 intron variant A/G snv 0.69
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 3 2014 2016
dbSNP: rs2427308
rs2427308
0.790 0.080 20 62394395 intron variant C/T snv 0.22
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 3 2014 2019
dbSNP: rs2450115
rs2450115
0.790 0.080 8 116611854 intergenic variant T/C snv 0.19
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 3 2016 2019
dbSNP: rs2735940
rs2735940
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 3 2019 2019
dbSNP: rs4444235
rs4444235
0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 3 2008 2019
dbSNP: rs4813802
rs4813802
0.776 0.080 20 6718948 regulatory region variant T/G snv 0.28
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 3 2019 2019
dbSNP: rs6469656
rs6469656
0.790 0.080 8 116635549 regulatory region variant G/A;C snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 3 2014 2019
dbSNP: rs7014346
rs7014346
0.732 0.240 8 127412547 intron variant A/G snv 0.63
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 3 2008 2016
dbSNP: rs73376930
rs73376930
0.790 0.080 15 32720301 intron variant A/G snv 0.25
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 3 2014 2019
dbSNP: rs1035209
rs1035209
0.790 0.080 10 99585609 intergenic variant C/T snv 0.15
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2014 2019
dbSNP: rs10849432
rs10849432
0.790 0.080 12 6276561 intergenic variant C/T snv 0.84
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2014 2016
dbSNP: rs10911251
rs10911251
0.790 0.080 1 183112059 intron variant A/C snv 0.37
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2013 2019
dbSNP: rs11874392
rs11874392
0.763 0.080 18 48926786 intron variant A/T snv 0.50
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2016 2019
dbSNP: rs12412391
rs12412391
0.790 0.080 10 99529178 intron variant A/G;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2014 2016
dbSNP: rs12603526
rs12603526
NXN
0.790 0.080 17 897353 intron variant T/C snv 2.3E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2014 2016
dbSNP: rs1321311
rs1321311
0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2012 2019
dbSNP: rs16878812
rs16878812
0.776 0.080 6 35601785 intron variant A/G snv 0.15
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2019 2019
dbSNP: rs17094983
rs17094983
0.776 0.080 14 58722643 intron variant G/A snv 0.12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2019 2019
dbSNP: rs1741640
rs1741640
0.776 0.080 20 62357358 intron variant T/C snv 0.66
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2019 2019
dbSNP: rs17816465
rs17816465
0.776 0.080 15 32864185 intron variant G/A snv 0.15
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2019 2019
dbSNP: rs1810502
rs1810502
0.790 0.080 20 50440951 intergenic variant C/T snv 0.49
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2019 2019
dbSNP: rs3087967
rs3087967
0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2019 2019
dbSNP: rs35107139
rs35107139
0.776 0.080 14 53952388 intron variant A/C;G;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2019 2019
dbSNP: rs35360328
rs35360328
0.790 0.080 3 40883471 intergenic variant T/A snv 0.11
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 2 2015 2019