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rs869025314

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025314(C;T)
Make rs869025314(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position66262055
GeneSLC25A26
is asnp
is mentioned by
dbSNPrs869025314
ebirs869025314
HLIrs869025314
Exacrs869025314
Varsomers869025314
Maprs869025314
PheGenIrs869025314
hapmaprs869025314
1000 genomesrs869025314
hgdprs869025314
ensemblrs869025314
gopubmedrs869025314
geneviewrs869025314
scholarrs869025314
googlers869025314
pharmgkbrs869025314
gwascentralrs869025314
openSNPrs869025314
23andMers869025314
23andMe allrs869025314
SNP Nexus

SNPshotrs869025314
SNPdbers869025314
MSV3drs869025314
GWAS Ctlgrs869025314
Max Magnitude0
ClinVar
Risk rs869025314(T;T)
Alt rs869025314(T;T)
Reference rs869025314(C;C)
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.66312479C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000207457.1,