Source: ALL
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: rs79007183
rs79007183
1.000 0.040 16 1655793 intron variant G/A snv 2.8E-05
CUI: C0014544
Disease: Epilepsy
Epilepsy
Nervous System Diseases 0.700 1.000 1 2015 2015