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rs267607098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607098(C;T)
Make rs267607098(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position84441330
GeneSUCLG1
is asnp
is mentioned by
dbSNPrs267607098
ebirs267607098
HLIrs267607098
Exacrs267607098
Varsomers267607098
Maprs267607098
PheGenIrs267607098
hapmaprs267607098
1000 genomesrs267607098
hgdprs267607098
ensemblrs267607098
gopubmedrs267607098
geneviewrs267607098
scholarrs267607098
googlers267607098
pharmgkbrs267607098
gwascentralrs267607098
openSNPrs267607098
23andMers267607098
23andMe allrs267607098
SNP Nexus

SNPshotrs267607098
SNPdbers267607098
MSV3drs267607098
GWAS Ctlgrs267607098
Max Magnitude0
ClinVar
Risk rs267607098(T;T)
Alt rs267607098(T;T)
Reference rs267607098(C;C)
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.84668454G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001043.3,