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: rs658191
rs658191
0.790 0.080 1 39458103 non coding transcript exon variant C/G snv 6.1E-02
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs658191
rs658191
0.790 0.080 1 39458103 non coding transcript exon variant C/G snv 6.1E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2016 2016
dbSNP: rs7528276
rs7528276
0.790 0.080 1 39344315 intron variant T/A;C snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs7528276
rs7528276
0.790 0.080 1 39344315 intron variant T/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.710 1.000 1 2016 2016
dbSNP: rs7528276
rs7528276
0.790 0.080 1 39344315 intron variant T/A;C snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2016 2016
dbSNP: rs7528276
rs7528276
0.790 0.080 1 39344315 intron variant T/A;C snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2016 2016
dbSNP: rs7528276
rs7528276
0.790 0.080 1 39344315 intron variant T/A;C snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs7528276
rs7528276
0.790 0.080 1 39344315 intron variant T/A;C snv
Malignant neoplasm of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs7528276
rs7528276
0.790 0.080 1 39344315 intron variant T/A;C snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2016 2016
dbSNP: rs7528276
rs7528276
0.790 0.080 1 39344315 intron variant T/A;C snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs7528276
rs7528276
0.790 0.080 1 39344315 intron variant T/A;C snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2016 2016