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rs267607099

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607099(C;G)
Make rs267607099(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position84441269
GeneSUCLG1
is asnp
is mentioned by
dbSNPrs267607099
ebirs267607099
HLIrs267607099
Exacrs267607099
Varsomers267607099
Maprs267607099
PheGenIrs267607099
hapmaprs267607099
1000 genomesrs267607099
hgdprs267607099
ensemblrs267607099
gopubmedrs267607099
geneviewrs267607099
scholarrs267607099
googlers267607099
pharmgkbrs267607099
gwascentralrs267607099
openSNPrs267607099
23andMers267607099
23andMe allrs267607099
SNP Nexus

SNPshotrs267607099
SNPdbers267607099
MSV3drs267607099
GWAS Ctlgrs267607099
Max Magnitude0
ClinVar
Risk rs267607099(G;G)
Alt rs267607099(G;G)
Reference rs267607099(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.84668393G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001041.3,