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rs587778772

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778772(-;-)
Make rs587778772(-;CTC)
Make rs587778772(CTC;CTC)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position41966738
GeneATP1A3
is asnp
is mentioned by
dbSNPrs587778772
ebirs587778772
HLIrs587778772
Exacrs587778772
Varsomers587778772
Maprs587778772
PheGenIrs587778772
hapmaprs587778772
1000 genomesrs587778772
hgdprs587778772
ensemblrs587778772
gopubmedrs587778772
geneviewrs587778772
scholarrs587778772
googlers587778772
pharmgkbrs587778772
gwascentralrs587778772
openSNPrs587778772
23andMers587778772
23andMe allrs587778772
SNP Nexus

SNPshotrs587778772
SNPdbers587778772
MSV3drs587778772
GWAS Ctlgrs587778772
Max Magnitude0
ClinVar
Risk rs587778772(CTC;CTC)
Alt rs587778772(CTC;CTC)
Reference rs587778772(;)
Significance Pathogenic
Disease Dystonia 12
Variation info
Gene ATP1A3
CLNDBN Dystonia 12
Reversed 1
HGVS NC_000019.9:g.42470891_42470893dupGAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000013779.20,