Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Migraine, Familial Hemiplegic, 3
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
14 0.851 0.080 2 165998049 missense variant G/T snv 0.800 1.000 4 2005 2009
Hemiplegic migraine, familial type 1
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
37 0.851 0.080 2 165998049 missense variant G/T snv 0.020 1.000 2 2008 2013
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.851 0.080 2 165998049 missense variant G/T snv 0.010 1.000 1 2005 2005
Epilepsy, Generalized
CUI: C0014548
Disease: Epilepsy, Generalized
36 0.851 0.080 2 165998049 missense variant G/T snv 0.010 1.000 1 2008 2008
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.851 0.080 2 165998049 missense variant G/T snv 0.010 1.000 1 2008 2008