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: rs4909945
rs4909945
11 10652192 missense variant T/A;C snv 0.76
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
Nervous System Diseases 0.800 1.000 1 2013 2013
dbSNP: rs4910165
rs4910165
11 10652497 intron variant C/G snv 0.78
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
Nervous System Diseases 0.700 1.000 2 2016 2016