rs1058808, ERBB2

N. diseases: 27
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.
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 0.010 1.000 1 2019 2019
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 0.010 1.000 1 2016 2016