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: rs121918799
rs121918799
0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine
Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1253956567
rs1253956567
1.000 0.040 2 166038072 missense variant C/G;T snv 4.0E-06; 8.0E-06
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine
Nervous System Diseases 0.010 1.000 1 2014 2014