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.
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.807 0.120 17 39724747 missense variant G/A;C;T snv 0.700 1.000 4 2011 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.807 0.120 17 39724747 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.807 0.120 17 39724747 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.807 0.120 17 39724747 missense variant G/A;C;T snv 0.030 1.000 3 2017 2019
HER2 gene amplification
CUI: C1512127
Disease: HER2 gene amplification
14 0.807 0.120 17 39724747 missense variant G/A;C;T snv 0.030 0.667 3 2016 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.807 0.120 17 39724747 missense variant G/A;C;T snv 0.030 1.000 3 2017 2019
Carcinoma breast stage IV
CUI: C0278488
Disease: Carcinoma breast stage IV
14 0.807 0.120 17 39724747 missense variant G/A;C;T snv 0.010 1.000 1 2019 2019
Luminal B Breast Carcinoma
CUI: C3642346
Disease: Luminal B Breast Carcinoma
7 0.807 0.120 17 39724747 missense variant G/A;C;T snv 0.010 1.000 1 2019 2019