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rs573535377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs573535377(G;T)
Make rs573535377(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position41981991
GeneATP1A3
is asnp
is mentioned by
dbSNPrs573535377
dbSNP (old)rs573535377
ClinGenrs573535377
ebirs573535377
HLIrs573535377
Exacrs573535377
Gnomadrs573535377
Varsomers573535377
Maprs573535377
PheGenIrs573535377
Biobankrs573535377
1000 genomesrs573535377
hgdprs573535377
ensemblrs573535377
gopubmedrs573535377
geneviewrs573535377
scholarrs573535377
googlers573535377
pharmgkbrs573535377
gwascentralrs573535377
openSNPrs573535377
23andMers573535377
23andMe allrs573535377
SNP Nexus

SNPshotrs573535377
SNPdbers573535377
MSV3drs573535377
GWAS Ctlgrs573535377
Max Magnitude0
ClinVar
Risk rs573535377(T;T)
Alt rs573535377(T;T)
Reference Rs573535377(G;G)
Significance Pathogenic
Disease Dystonia 12
Variation info
Gene ATP1A3
CLNDBN Dystonia 12
Reversed 0
HGVS NC_000019.9:g.42486143G>T
CLNSRC ClinVar
CLNACC RCV000148336.1,