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: rs9566845
rs9566845
0.925 0.040 13 41761944 intron variant G/A snv 6.1E-02
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs9566867
rs9566867
13 41854763 intron variant G/A snv 6.2E-02
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
Nervous System Diseases 0.010 1.000 1 2010 2010