rs1057519943, POLE

N. diseases: 10
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 of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.790 0.160 12 132676598 missense variant G/C;T snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.790 0.160 12 132676598 missense variant G/C;T snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.790 0.160 12 132676598 missense variant G/C;T snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.790 0.160 12 132676598 missense variant G/C;T snv 0.700 1.000 1 2016 2016
Uterine Carcinosarcoma
CUI: C0280630
Disease: Uterine Carcinosarcoma
80 0.790 0.160 12 132676598 missense variant G/C;T snv 0.700 1.000 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.790 0.160 12 132676598 missense variant G/C;T snv 0.020 1.000 2 2018 2019
Carcinoma, Endometrioid
CUI: C0206687
Disease: Carcinoma, Endometrioid
12 0.790 0.160 12 132676598 missense variant G/C;T snv 0.010 1.000 1 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.790 0.160 12 132676598 missense variant G/C;T snv 0.010 1.000 1 2016 2016
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.790 0.160 12 132676598 missense variant G/C;T snv 0.010 1.000 1 2016 2016
Undifferentiated carcinoma
CUI: C0205698
Disease: Undifferentiated carcinoma
8 0.790 0.160 12 132676598 missense variant G/C;T snv 0.010 1.000 1 2018 2018