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 1.000 0.040 2 166036257 missense variant C/T snv 4.0E-06 2.1E-05 0.020 1.000 2 2009 2017