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: rs4814864
rs4814864
20 19489173 intron variant G/C;T snv
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs6081613
rs6081613
20 19485263 intron variant G/A snv 0.25
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
Nervous System Diseases 0.700 1.000 1 2016 2016