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rs869025313

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025313(G;G)
Make rs869025313(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position66263369
GeneSLC25A26
is asnp
is mentioned by
dbSNPrs869025313
ebirs869025313
HLIrs869025313
Exacrs869025313
Varsomers869025313
Maprs869025313
PheGenIrs869025313
hapmaprs869025313
1000 genomesrs869025313
hgdprs869025313
ensemblrs869025313
gopubmedrs869025313
geneviewrs869025313
scholarrs869025313
googlers869025313
pharmgkbrs869025313
gwascentralrs869025313
openSNPrs869025313
23andMers869025313
23andMe allrs869025313
SNP Nexus

SNPshotrs869025313
SNPdbers869025313
MSV3drs869025313
GWAS Ctlgrs869025313
Max Magnitude0
ClinVar
Risk rs869025313(G;G)
Alt rs869025313(G;G)
Reference rs869025313(T;T)
Significance Pathogenic
Disease Combined oxidative phosphorylation deficiency 28
Variation info
Gene SLC25A26
CLNDBN Combined oxidative phosphorylation deficiency 28
Reversed 0
HGVS NC_000003.11:g.66313793T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000207467.1,