Disease: MIGRAINE, SPORADIC HEMIPLEGIC ×
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: rs1553245771
rs1553245771 		0.882 0.040 1 160135461 missense variant G/A snv
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		Nervous System Diseases 0.010 1.000 1 2011 2011