Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2029461
rs2029461
1.000 0.040 6 34138013 intron variant C/T snv 0.43
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy
Nervous System Diseases 0.010 1.000 1 2017 2017