rs746795369, ATP1A2

N. diseases: 6
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, 2
CUI: C1865322
Disease: MIGRAINE, FAMILIAL HEMIPLEGIC, 2
14 0.827 0.080 1 160139969 missense variant C/A;T snv 1.2E-05; 4.0E-06 0.700 1.000 5 2003 2014
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.827 0.080 1 160139969 missense variant C/A;T snv 1.2E-05; 4.0E-06 0.010 1.000 1 2013 2013
Familial Hemiplegic Migraine
CUI: C0338484
Disease: Familial Hemiplegic Migraine
17 0.827 0.080 1 160139969 missense variant C/A;T snv 1.2E-05; 4.0E-06 0.010 1.000 1 2013 2013
Hemiplegic migraine
CUI: C0270862
Disease: Hemiplegic migraine
14 0.827 0.080 1 160139969 missense variant C/A;T snv 1.2E-05; 4.0E-06 0.010 1.000 1 2013 2013
Hemiplegic migraine, familial type 1
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
37 0.827 0.080 1 160139969 missense variant C/A;T snv 1.2E-05; 4.0E-06 0.010 1.000 1 2013 2013
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.827 0.080 1 160139969 missense variant C/A;T snv 1.2E-05; 4.0E-06 0.010 1.000 1 2013 2013