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rs606231435

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231435(A;A)
Make rs606231435(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position41970539
GeneATP1A3
is asnp
is mentioned by
dbSNPrs606231435
ebirs606231435
HLIrs606231435
Exacrs606231435
Varsomers606231435
Maprs606231435
PheGenIrs606231435
hapmaprs606231435
1000 genomesrs606231435
hgdprs606231435
ensemblrs606231435
gopubmedrs606231435
geneviewrs606231435
scholarrs606231435
googlers606231435
pharmgkbrs606231435
gwascentralrs606231435
openSNPrs606231435
23andMers606231435
23andMe allrs606231435
SNP Nexus

SNPshotrs606231435
SNPdbers606231435
MSV3drs606231435
GWAS Ctlgrs606231435
Max Magnitude0
ClinVar
Risk rs606231435(A;A)
Alt rs606231435(A;A)
Reference rs606231435(G;G)
Significance Pathogenic
Disease Dystonia 12
Variation info
Gene ATP1A3
CLNDBN Dystonia 12
Reversed 1
HGVS NC_000019.9:g.42474691C>T
CLNSRC
CLNACC RCV000148315.1,