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rs606231440

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231440(A;T)
Make rs606231440(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position41970299
GeneATP1A3
is asnp
is mentioned by
dbSNPrs606231440
ebirs606231440
HLIrs606231440
Exacrs606231440
Varsomers606231440
Maprs606231440
PheGenIrs606231440
hapmaprs606231440
1000 genomesrs606231440
hgdprs606231440
ensemblrs606231440
gopubmedrs606231440
geneviewrs606231440
scholarrs606231440
googlers606231440
pharmgkbrs606231440
gwascentralrs606231440
openSNPrs606231440
23andMers606231440
23andMe allrs606231440
SNP Nexus

SNPshotrs606231440
SNPdbers606231440
MSV3drs606231440
GWAS Ctlgrs606231440
Max Magnitude0
ClinVar
Risk rs606231440(T;T)
Alt rs606231440(T;T)
Reference rs606231440(A;A)
Significance Pathogenic
Disease Alternating hemiplegia of childhood 2
Variation info
Gene ATP1A3
CLNDBN Alternating hemiplegia of childhood 2
Reversed 1
HGVS NC_000019.9:g.42474451T>A
CLNSRC
CLNACC RCV000148324.1,