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rs387906731

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906731(A;G)
Make rs387906731(G;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position10450
GeneRPL23P3
is asnp
is mentioned by
dbSNPrs387906731
ebirs387906731
HLIrs387906731
Exacrs387906731
Varsomers387906731
Maprs387906731
PheGenIrs387906731
hapmaprs387906731
1000 genomesrs387906731
hgdprs387906731
ensemblrs387906731
gopubmedrs387906731
geneviewrs387906731
scholarrs387906731
googlers387906731
pharmgkbrs387906731
gwascentralrs387906731
openSNPrs387906731
23andMers387906731
23andMe allrs387906731
SNP Nexus

SNPshotrs387906731
SNPdbers387906731
MSV3drs387906731
GWAS Ctlgrs387906731
Max Magnitude0
ClinVar
Risk rs387906731(G;G)
Alt rs387906731(G;G)
Reference rs387906731(A;A)
Significance Pathogenic
Disease Mitochondrial encephalomyopathy
Variation info
Gene
CLNDBN Mitochondrial encephalomyopathy
Reversed 0
HGVS NC_012920.1:m.10450A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022895.4,