rs121913468, ERBB2

N. diseases: 7
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 0.827 0.160 17 39724008 missense variant G/A;C;T snv 0.700 1.000 4 2006 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.827 0.160 17 39724008 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.827 0.160 17 39724008 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
158 0.827 0.160 17 39724008 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
72 0.827 0.160 17 39724008 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.827 0.160 17 39724008 missense variant G/A;C;T snv 0.030 1.000 3 2015 2018
HER2 gene amplification
CUI: C1512127
Disease: HER2 gene amplification
14 0.827 0.160 17 39724008 missense variant G/A;C;T snv 0.010 1 2016 2016