Source: ALL
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: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.100 0.933 15 2007 2019
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 14 2007 2019
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 14 2007 2019
dbSNP: rs10505477
rs10505477 		0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 4 2007 2018
dbSNP: rs10505477
rs10505477 		0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 4 2007 2018
dbSNP: rs10505477
rs10505477 		0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 4 2007 2018
dbSNP: rs10505477
rs10505477 		0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 4 2007 2018
dbSNP: rs10505477
rs10505477 		0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.030 1.000 3 2014 2018
dbSNP: rs7014346
rs7014346 		0.732 0.240 8 127412547 intron variant A/G snv 0.63
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 3 2008 2016
dbSNP: rs7014346
rs7014346 		0.732 0.240 8 127412547 intron variant A/G snv 0.63
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 3 2008 2016
dbSNP: rs7014346
rs7014346 		0.732 0.240 8 127412547 intron variant A/G snv 0.63
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 3 2008 2016
dbSNP: rs7014346
rs7014346 		0.732 0.240 8 127412547 intron variant A/G snv 0.63
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 3 2008 2016
dbSNP: rs13256367
rs13256367 		8 127322655 intron variant A/C;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 2 2018 2019
dbSNP: rs10505477
rs10505477 		0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		0.700 1.000 1 2017 2017
dbSNP: rs10808556
rs10808556 		0.925 0.080 8 127400902 non coding transcript exon variant C/T snv 0.50
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
Differentiated Thyroid Gland Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2018 2018
dbSNP: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2018 2018
dbSNP: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2018 2018
dbSNP: rs12682374
rs12682374 		0.790 0.080 8 127398703 intron variant C/A;G;T snv
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs13281615
rs13281615 		0.716 0.360 8 127343372 intron variant A/G snv 0.43
CUI: C1096616
Disease: Contralateral breast cancer
Contralateral breast cancer 		0.010 1.000 1 2011 2011
dbSNP: rs1456315
rs1456315 		0.790 0.200 8 127091692 non coding transcript exon variant T/A;C snv
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2019 2019
dbSNP: rs17464492
rs17464492 		8 127330621 intron variant A/G snv 0.25
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		0.700 1.000 1 2017 2017
dbSNP: rs1906223
rs1906223 		8 126921448 intron variant C/T snv 0.29
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019