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rs869025315

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025315(C;T)
Make rs869025315(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position66369505
GeneSLC25A26
is asnp
is mentioned by
dbSNPrs869025315
ebirs869025315
HLIrs869025315
Exacrs869025315
Varsomers869025315
Maprs869025315
PheGenIrs869025315
hapmaprs869025315
1000 genomesrs869025315
hgdprs869025315
ensemblrs869025315
gopubmedrs869025315
geneviewrs869025315
scholarrs869025315
googlers869025315
pharmgkbrs869025315
gwascentralrs869025315
openSNPrs869025315
23andMers869025315
23andMe allrs869025315
SNP Nexus

SNPshotrs869025315
SNPdbers869025315
MSV3drs869025315
GWAS Ctlgrs869025315
Max Magnitude0
ClinVar
Risk rs869025315(T;T)
Alt rs869025315(T;T)
Reference rs869025315(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.66419929C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000207463.1,