Have questions? Visit https://www.reddit.com/r/SNPedia

rs397515577

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515577(C;T)
Make rs397515577(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position41976459
GeneATP1A3
is asnp
is mentioned by
dbSNPrs397515577
ebirs397515577
HLIrs397515577
Exacrs397515577
Varsomers397515577
Maprs397515577
PheGenIrs397515577
hapmaprs397515577
1000 genomesrs397515577
hgdprs397515577
ensemblrs397515577
gopubmedrs397515577
geneviewrs397515577
scholarrs397515577
googlers397515577
pharmgkbrs397515577
gwascentralrs397515577
openSNPrs397515577
23andMers397515577
23andMe allrs397515577
SNP Nexus

SNPshotrs397515577
SNPdbers397515577
MSV3drs397515577
GWAS Ctlgrs397515577
Max Magnitude0
ClinVar
Risk rs397515577(T;T)
Alt rs397515577(T;T)
Reference rs397515577(C;C)
Significance Pathogenic
Disease Dystonia 12
Variation info
Gene ATP1A3
CLNDBN Dystonia 12
Reversed 1
HGVS NC_000019.9:g.42480611G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000055992.2,