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rs606231439

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231439(C;G)
Make rs606231439(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position41970391
GeneATP1A3
is asnp
is mentioned by
dbSNPrs606231439
ebirs606231439
HLIrs606231439
Exacrs606231439
Varsomers606231439
Maprs606231439
PheGenIrs606231439
hapmaprs606231439
1000 genomesrs606231439
hgdprs606231439
ensemblrs606231439
gopubmedrs606231439
geneviewrs606231439
scholarrs606231439
googlers606231439
pharmgkbrs606231439
gwascentralrs606231439
openSNPrs606231439
23andMers606231439
23andMe allrs606231439
SNP Nexus

SNPshotrs606231439
SNPdbers606231439
MSV3drs606231439
GWAS Ctlgrs606231439
Max Magnitude0
ClinVar
Risk rs606231439(G;G)
Alt rs606231439(G;G)
Reference rs606231439(C;C)
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.42474543G>C
CLNSRC
CLNACC RCV000148322.1,