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rs606231448

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs606231448(C;C)
Make rs606231448(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position41981956
GeneATP1A3
is asnp
is mentioned by
dbSNPrs606231448
ebirs606231448
HLIrs606231448
Exacrs606231448
Varsomers606231448
Maprs606231448
PheGenIrs606231448
hapmaprs606231448
1000 genomesrs606231448
hgdprs606231448
ensemblrs606231448
gopubmedrs606231448
geneviewrs606231448
scholarrs606231448
googlers606231448
pharmgkbrs606231448
gwascentralrs606231448
openSNPrs606231448
23andMers606231448
23andMe allrs606231448
SNP Nexus

SNPshotrs606231448
SNPdbers606231448
MSV3drs606231448
GWAS Ctlgrs606231448
Max Magnitude0
ClinVar
Risk rs606231448(C;C)
Alt rs606231448(C;C)
Reference rs606231448(T;T)
Significance Pathogenic
Disease Dystonia 12
Variation info
Gene ATP1A3
CLNDBN Dystonia 12
Reversed 1
HGVS NC_000019.9:g.42486108A>G
CLNSRC
CLNACC RCV000148337.1,