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 0.240 8 127412547 intron variant A/G snv 0.63 0.830 0.889 9 2008 2019
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.710 1.000 3 2008 2015
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.700 1.000 3 2008 2016
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.700 1.000 3 2008 2016
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.700 1.000 3 2008 2016
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.700 1.000 3 2008 2016
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.700 1.000 3 2008 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.700 1.000 3 2008 2016
Malignant neoplasm of large intestine
375 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.700 1.000 3 2008 2016
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.700 1.000 3 2008 2016
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.700 1.000 1 2010 2010
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.010 1.000 1 2013 2013
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.010 1.000 1 2013 2013
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.732 0.240 8 127412547 intron variant A/G snv 0.63 0.010 1.000 1 2015 2015