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: rs121918632
rs121918632
0.851 0.120 2 165996099 missense variant A/G snv 7.0E-06
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine
Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs121918799
rs121918799
0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine
Nervous System Diseases 0.010 1.000 1 2013 2013