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rs387906736

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906736(A;A)
Make rs387906736(A;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position5556
GeneSMR3B
is asnp
is mentioned by
dbSNPrs387906736
ebirs387906736
HLIrs387906736
Exacrs387906736
Varsomers387906736
Maprs387906736
PheGenIrs387906736
hapmaprs387906736
1000 genomesrs387906736
hgdprs387906736
ensemblrs387906736
gopubmedrs387906736
geneviewrs387906736
scholarrs387906736
googlers387906736
pharmgkbrs387906736
gwascentralrs387906736
openSNPrs387906736
23andMers387906736
23andMe allrs387906736
SNP Nexus

SNPshotrs387906736
SNPdbers387906736
MSV3drs387906736
GWAS Ctlgrs387906736
Max Magnitude0
ClinVar
Risk rs387906736(A;A)
Alt rs387906736(A;A)
Reference rs387906736(G;G)
Significance Pathogenic
Disease Mitochondrial encephalomyopathy
Variation info
Gene
CLNDBN Mitochondrial encephalomyopathy
Reversed 0
HGVS NC_012920.1:m.5556G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022907.2,