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: rs121908217
rs121908217
0.851 0.120 19 13308452 missense variant C/T snv 4.0E-06
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC
Nervous System Diseases 0.710 1.000 1 2002 2002
dbSNP: rs121908212
rs121908212
0.732 0.160 19 13303877 missense variant G/A snv
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC
Nervous System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs121908225
rs121908225
0.790 0.120 19 13365448 missense variant G/A snv
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC
Nervous System Diseases 0.010 1.000 1 2006 2006