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: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.810 0.500 2 2011 2013
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.710 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2015 2015
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2016 2016
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm 		0.010 1.000 1 2017 2017
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 < 0.001 1 2013 2013
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		0.010 1.000 1 2017 2017