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rs549006436

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs549006436(A;T)
Make rs549006436(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position41970389
GeneATP1A3
is asnp
is mentioned by
dbSNPrs549006436
ebirs549006436
HLIrs549006436
Exacrs549006436
Varsomers549006436
Maprs549006436
PheGenIrs549006436
hapmaprs549006436
1000 genomesrs549006436
hgdprs549006436
ensemblrs549006436
gopubmedrs549006436
geneviewrs549006436
scholarrs549006436
googlers549006436
pharmgkbrs549006436
gwascentralrs549006436
openSNPrs549006436
23andMers549006436
23andMe allrs549006436
SNP Nexus

SNPshotrs549006436
SNPdbers549006436
MSV3drs549006436
GWAS Ctlgrs549006436
Max Magnitude0
ClinVar
Risk rs549006436(C,T;C,T)
Alt rs549006436(C,T;C,T)
Reference rs549006436(A;A)
Significance Pathogenic
Disease Alternating hemiplegia of childhood 2
Variation info
Gene ATP1A3
CLNDBN Alternating hemiplegia of childhood 2
Reversed 0
HGVS NC_000019.9:g.42474541A>C
CLNSRC ClinVar
CLNACC RCV000148323.1,