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: rs121908225
rs121908225
0.790 0.120 19 13365448 missense variant G/A snv
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine
Nervous System Diseases 0.030 1.000 3 2009 2018
dbSNP: rs1057520918
rs1057520918
0.790 0.160 19 13262780 missense variant C/T snv
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine
Nervous System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1164174661
rs1164174661
0.925 0.120 19 13283358 missense variant T/C snv
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine
Nervous System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs121908212
rs121908212
0.732 0.160 19 13303877 missense variant G/A snv
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine
Nervous System Diseases 0.010 1.000 1 2004 2004
dbSNP: rs121908217
rs121908217
0.851 0.120 19 13308452 missense variant C/T snv 4.0E-06
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine
Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs121908230
rs121908230
0.882 0.080 19 13262789 missense variant C/T snv
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine
Nervous System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs763054302
rs763054302
1.000 0.040 19 13299007 missense variant C/T snv 8.5E-05 4.9E-05
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine
Nervous System Diseases 0.010 1.000 1 2014 2014