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: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine
Nervous System Diseases 0.040 1.000 4 2008 2011
dbSNP: rs121908211
rs121908211
0.882 0.080 19 13371744 missense variant C/T snv
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine
Nervous System Diseases 0.030 1.000 3 2005 2015
dbSNP: rs121908212
rs121908212
0.732 0.160 19 13303877 missense variant G/A snv
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine
Nervous System Diseases 0.030 1.000 3 1999 2019
dbSNP: rs121908214
rs121908214
0.925 0.080 19 13230185 missense variant T/G snv
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine
Nervous System Diseases 0.010 1.000 1 2004 2004
dbSNP: rs121908218
rs121908218
0.925 0.080 19 13303576 missense variant G/A;C;T snv
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine
Nervous System Diseases 0.010 1.000 1 1999 1999
dbSNP: rs121908223
rs121908223
0.925 0.080 19 13262823 missense variant T/C snv
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine
Nervous System Diseases 0.010 1.000 1 2013 2013