rs7758229, SLC22A3

N. diseases: 16
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.732 0.120 6 160419220 intron variant G/A;T snv 0.810 0.500 2 2011 2013
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.732 0.120 6 160419220 intron variant G/A;T snv 0.710 1.000 1 2011 2011
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.732 0.120 6 160419220 intron variant G/A;T snv 0.700 1.000 1 2011 2011
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.732 0.120 6 160419220 intron variant G/A;T snv 0.700 1.000 1 2011 2011
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.732 0.120 6 160419220 intron variant G/A;T snv 0.700 1.000 1 2011 2011
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.732 0.120 6 160419220 intron variant G/A;T snv 0.700 1.000 1 2011 2011
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.732 0.120 6 160419220 intron variant G/A;T snv 0.700 1.000 1 2011 2011
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.732 0.120 6 160419220 intron variant G/A;T snv 0.700 1.000 1 2011 2011
Malignant neoplasm of large intestine
375 0.732 0.120 6 160419220 intron variant G/A;T snv 0.700 1.000 1 2011 2011
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.732 0.120 6 160419220 intron variant G/A;T snv 0.700 1.000 1 2015 2015
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.732 0.120 6 160419220 intron variant G/A;T snv 0.010 1.000 1 2011 2011
Malignant neoplasm of colon and/or rectum
502 0.732 0.120 6 160419220 intron variant G/A;T snv 0.010 1 2013 2013
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.732 0.120 6 160419220 intron variant G/A;T snv 0.010 1.000 1 2016 2016
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.732 0.120 6 160419220 intron variant G/A;T snv 0.010 1.000 1 2017 2017
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.732 0.120 6 160419220 intron variant G/A;T snv 0.010 1.000 1 2017 2017
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.732 0.120 6 160419220 intron variant G/A;T snv 0.010 1.000 1 2016 2016