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rs267607097

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607097(C;C)
Make rs267607097(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position84443348
GeneSUCLG1
is asnp
is mentioned by
dbSNPrs267607097
ebirs267607097
HLIrs267607097
Exacrs267607097
Varsomers267607097
Maprs267607097
PheGenIrs267607097
hapmaprs267607097
1000 genomesrs267607097
hgdprs267607097
ensemblrs267607097
gopubmedrs267607097
geneviewrs267607097
scholarrs267607097
googlers267607097
pharmgkbrs267607097
gwascentralrs267607097
openSNPrs267607097
23andMers267607097
23andMe allrs267607097
SNP Nexus

SNPshotrs267607097
SNPdbers267607097
MSV3drs267607097
GWAS Ctlgrs267607097
Max Magnitude0
ClinVar
Risk rs267607097(C;C)
Alt rs267607097(C;C)
Reference rs267607097(G;G)
Significance Pathogenic
Disease Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria)
Variation info
Gene SUCLG1
CLNDBN Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria)
Reversed 1
HGVS NC_000002.11:g.84670472C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001040.3,