rs443198, NOTCH4

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.
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.851 0.200 6 32222629 synonymous variant A/G snv 0.38 0.39 0.010 1.000 1 2017 2017