rs11506105, EGFR

N. diseases: 4
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.
Glioma
CUI: C0017638
Disease: Glioma
353 0.851 0.160 7 55152484 intron variant A/G snv 0.59 0.010 1.000 1 2017 2017
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.851 0.160 7 55152484 intron variant A/G snv 0.59 0.010 1.000 1 2015 2015
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.851 0.160 7 55152484 intron variant A/G snv 0.59 0.010 1.000 1 2017 2017
Pseudohyperkalemia Cardiff
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
60 0.851 0.160 7 55152484 intron variant A/G snv 0.59 0.010 1.000 1 2017 2017