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rs606231449

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs606231449(C;C)
Make rs606231449(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position41981774
GeneATP1A3
is asnp
is mentioned by
dbSNPrs606231449
ebirs606231449
HLIrs606231449
Exacrs606231449
Varsomers606231449
Maprs606231449
PheGenIrs606231449
hapmaprs606231449
1000 genomesrs606231449
hgdprs606231449
ensemblrs606231449
gopubmedrs606231449
geneviewrs606231449
scholarrs606231449
googlers606231449
pharmgkbrs606231449
gwascentralrs606231449
openSNPrs606231449
23andMers606231449
23andMe allrs606231449
SNP Nexus

SNPshotrs606231449
SNPdbers606231449
MSV3drs606231449
GWAS Ctlgrs606231449
Max Magnitude0
ClinVar
Risk rs606231449(C;C)
Alt rs606231449(C;C)
Reference rs606231449(T;T)
Significance Pathogenic
Disease Dystonia 12
Variation info
Gene ATP1A3
CLNDBN Dystonia 12
Reversed 1
HGVS NC_000019.9:g.42485926A>G
CLNSRC
CLNACC RCV000148338.1,