rs72823592, COPZ2

N. diseases: 2
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.
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.925 0.040 17 48045642 non coding transcript exon variant G/A;C snv 0.800 1.000 1 2012 2012
Epilepsy, Generalized
CUI: C0014548
Disease: Epilepsy, Generalized
36 0.925 0.040 17 48045642 non coding transcript exon variant G/A;C snv 0.010 1.000 1 2014 2014