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: rs12355831
rs12355831
10 112442768 intron variant A/G snv 7.9E-02
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2256368
rs2256368
10 112426866 splice region variant G/A snv 0.93 0.93
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
Nervous System Diseases 0.010 1.000 1 2016 2016