rs1057519893, ERBB3

N. diseases: 9
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 Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.790 0.160 12 56085070 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Gallbladder Carcinoma
CUI: C0235782
Disease: Gallbladder Carcinoma
75 0.790 0.160 12 56085070 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.790 0.160 12 56085070 missense variant G/A;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 56085070 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.790 0.160 12 56085070 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
158 0.790 0.160 12 56085070 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Uterine Carcinosarcoma
CUI: C0280630
Disease: Uterine Carcinosarcoma
80 0.790 0.160 12 56085070 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
72 0.790 0.160 12 56085070 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Ovarian Mucinous Adenocarcinoma
CUI: C1335167
Disease: Ovarian Mucinous Adenocarcinoma
24 0.790 0.160 12 56085070 missense variant G/A;T snv 0.700 0