rs587777771, ATP1A3

N. diseases: 4
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.
CAPOS syndrome
CUI: C1832466
Disease: CAPOS syndrome
11 0.851 0.240 19 41970275 missense variant C/T snv 0.870 1.000 8 2014 2019
DYSTONIA 12
CUI: C1868681
Disease: DYSTONIA 12
25 0.851 0.240 19 41970275 missense variant C/T snv 0.700 1.000 2 2014 2014
ALTERNATING HEMIPLEGIA OF CHILDHOOD 2
CUI: C3553788
Disease: ALTERNATING HEMIPLEGIA OF CHILDHOOD 2
38 0.851 0.240 19 41970275 missense variant C/T snv 0.700 0
Hemiplegic migraine
CUI: C0270862
Disease: Hemiplegic migraine
14 0.851 0.240 19 41970275 missense variant C/T snv 0.010 1.000 1 2015 2015