rs1057519890, ERBB2

N. diseases: 8
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 Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.807 0.200 17 39723966 missense variant T/A snv 0.010 1.000 1 2015 2015
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.807 0.200 17 39723966 missense variant T/A snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.807 0.200 17 39723966 missense variant T/A snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.807 0.200 17 39723966 missense variant T/A snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.807 0.200 17 39723966 missense variant T/A snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.807 0.200 17 39723966 missense variant T/A snv 0.700 1.000 1 2016 2016
Papillary renal cell carcinoma, sporadic
30 0.807 0.200 17 39723966 missense variant T/A snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
158 0.807 0.200 17 39723966 missense variant T/A snv 0.700 1.000 1 2016 2016