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rs121434410

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434410(C;T)
Make rs121434410(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178436264
GeneAC009948.5, PRKRA
is asnp
is mentioned by
dbSNPrs121434410
ebirs121434410
HLIrs121434410
Exacrs121434410
Varsomers121434410
Maprs121434410
PheGenIrs121434410
hapmaprs121434410
1000 genomesrs121434410
hgdprs121434410
ensemblrs121434410
gopubmedrs121434410
geneviewrs121434410
scholarrs121434410
googlers121434410
pharmgkbrs121434410
gwascentralrs121434410
openSNPrs121434410
23andMers121434410
23andMe allrs121434410
SNP Nexus

SNPshotrs121434410
SNPdbers121434410
MSV3drs121434410
GWAS Ctlgrs121434410
Max Magnitude0
OMIM603424
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434410(T;T)
Alt rs121434410(T;T)
Reference rs121434410(C;C)
Significance Pathogenic
Disease Dystonia 16
Variation info
Gene LOC101927027 PRKRA
CLNDBN Dystonia 16
Reversed 1
HGVS NC_000002.11:g.179300991G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006718.3,