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rs121434456

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121434456(A;G)
Make rs121434456(G;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position10438
GeneRPL23P3
is asnp
is mentioned by
dbSNPrs121434456
ebirs121434456
HLIrs121434456
Exacrs121434456
Varsomers121434456
Maprs121434456
PheGenIrs121434456
hapmaprs121434456
1000 genomesrs121434456
hgdprs121434456
ensemblrs121434456
gopubmedrs121434456
geneviewrs121434456
scholarrs121434456
googlers121434456
pharmgkbrs121434456
gwascentralrs121434456
openSNPrs121434456
23andMers121434456
23andMe allrs121434456
SNP Nexus

SNPshotrs121434456
SNPdbers121434456
MSV3drs121434456
GWAS Ctlgrs121434456
Max Magnitude0
ClinVar
Risk rs121434456(G;G)
Alt rs121434456(G;G)
Reference rs121434456(A;A)
Significance Pathogenic
Disease Mitochondrial encephalomyopathy
Variation info
Gene
CLNDBN Mitochondrial encephalomyopathy
Reversed 0
HGVS NC_012920.1:m.10438A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010249.2,