rs12645561, NEIL3

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.
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.882 0.120 4 177339718 intron variant C/A;T snv 0.010 1.000 1 2013 2013
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.882 0.120 4 177339718 intron variant C/A;T snv 0.010 1.000 1 2013 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.120 4 177339718 intron variant C/A;T snv 0.010 1.000 1 2015 2015