rs879255368, ATP1A3

N. diseases: 5
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.
Apnea
CUI: C0003578
Disease: Apnea
11 19 41984953 missense variant C/G;T snv 0.700 0
Delayed speech and language development
CUI: C0454644
Disease: Delayed speech and language development
192 19 41984953 missense variant C/G;T snv 0.700 0
Hemiplegia
CUI: C0018991
Disease: Hemiplegia
6 19 41984953 missense variant C/G;T snv 0.700 0
Oculogyric crisis
CUI: C0085637
Disease: Oculogyric crisis
3 19 41984953 missense variant C/G;T snv 0.700 0
Seizures
CUI: C0036572
Disease: Seizures
553 19 41984953 missense variant C/G;T snv 0.700 0