rs17172432, EGFR

N. diseases: 3
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 0.882 0.080 7 55073624 intron variant T/C snv 0.31 0.010 1 2017 2017
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.882 0.080 7 55073624 intron variant T/C snv 0.31 0.010 1.000 1 2013 2013
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.882 0.080 7 55073624 intron variant T/C snv 0.31 0.010 1.000 1 2013 2013