rs782503624, ATP1A3

N. diseases: 2
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 0.925 0.240 19 41970308 missense variant C/T snv 4.0E-06 0.040 1.000 4 2015 2019
Hemiplegic migraine
CUI: C0270862
Disease: Hemiplegic migraine
14 0.925 0.240 19 41970308 missense variant C/T snv 4.0E-06 0.010 1.000 1 2015 2015