Source: ALL

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: rs10411210
rs10411210
0.742 0.160 19 33041394 intron variant C/T snv 0.22
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.840 1.000 7 2008 2019
dbSNP: rs13343954
rs13343954
0.790 0.080 19 33036982 intron variant T/C snv 0.18
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 1.000 1 2014 2014
dbSNP: rs10411210
rs10411210
0.742 0.160 19 33041394 intron variant C/T snv 0.22
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.710 1.000 4 2008 2019
dbSNP: rs10411210
rs10411210
0.742 0.160 19 33041394 intron variant C/T snv 0.22
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 3 2008 2019
dbSNP: rs10411210
rs10411210
0.742 0.160 19 33041394 intron variant C/T snv 0.22
Malignant neoplasm of large intestine
0.700 1.000 3 2008 2019
dbSNP: rs10411210
rs10411210
0.742 0.160 19 33041394 intron variant C/T snv 0.22
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 3 2008 2019
dbSNP: rs10411210
rs10411210
0.742 0.160 19 33041394 intron variant C/T snv 0.22
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 3 2008 2019
dbSNP: rs10411210
rs10411210
0.742 0.160 19 33041394 intron variant C/T snv 0.22
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 3 2008 2019
dbSNP: rs10411210
rs10411210
0.742 0.160 19 33041394 intron variant C/T snv 0.22
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 3 2008 2019
dbSNP: rs10411210
rs10411210
0.742 0.160 19 33041394 intron variant C/T snv 0.22
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 3 2008 2019
dbSNP: rs10411210
rs10411210
0.742 0.160 19 33041394 intron variant C/T snv 0.22
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 1 2010 2010
dbSNP: rs13343954
rs13343954
0.790 0.080 19 33036982 intron variant T/C snv 0.18
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2014 2014
dbSNP: rs13343954
rs13343954
0.790 0.080 19 33036982 intron variant T/C snv 0.18
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2014 2014
dbSNP: rs13343954
rs13343954
0.790 0.080 19 33036982 intron variant T/C snv 0.18
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs13343954
rs13343954
0.790 0.080 19 33036982 intron variant T/C snv 0.18
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2014 2014
dbSNP: rs13343954
rs13343954
0.790 0.080 19 33036982 intron variant T/C snv 0.18
Malignant neoplasm of large intestine
0.700 1.000 1 2014 2014
dbSNP: rs13343954
rs13343954
0.790 0.080 19 33036982 intron variant T/C snv 0.18
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2014 2014
dbSNP: rs13343954
rs13343954
0.790 0.080 19 33036982 intron variant T/C snv 0.18
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.700 1.000 1 2014 2014
dbSNP: rs13343954
rs13343954
0.790 0.080 19 33036982 intron variant T/C snv 0.18
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2014 2014
dbSNP: rs28840750
rs28840750
0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs28840750
rs28840750
0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2019 2019
dbSNP: rs28840750
rs28840750
0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs28840750
rs28840750
0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs28840750
rs28840750
0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2019 2019
dbSNP: rs28840750
rs28840750
0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019