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.
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 4 2007 2018
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.010 1.000 1 2019 2019
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.020 1.000 2 2016 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.010 1.000 1 2015 2015
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 4 2007 2018
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 4 2007 2018
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 4 2007 2018
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 4 2007 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.890 0.938 16 2007 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 4 2007 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.010 1.000 1 2015 2015
Malignant neoplasm of colon and/or rectum
502 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.030 1.000 3 2014 2018
Malignant neoplasm of large intestine
375 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 4 2007 2018
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 2 2008 2013
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.040 1.000 4 2014 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.010 1.000 1 2018 2018
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 4 2007 2018
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 1 2010 2010
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016