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rs886041081

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome4
Position185144891
GeneSLC25A4
is asnp
is mentioned by
dbSNPrs886041081
dbSNP (classic)rs886041081
ClinGenrs886041081
ebirs886041081
HLIrs886041081
Exacrs886041081
Gnomadrs886041081
Varsomers886041081
LitVarrs886041081
Maprs886041081
PheGenIrs886041081
Biobankrs886041081
1000 genomesrs886041081
hgdprs886041081
ensemblrs886041081
geneviewrs886041081
scholarrs886041081
googlers886041081
pharmgkbrs886041081
gwascentralrs886041081
openSNPrs886041081
23andMers886041081
SNPshotrs886041081
SNPdbers886041081
MSV3drs886041081
GWAS Ctlgrs886041081
Max Magnitude0
ClinVar
Risk rs886041081(A;A)
Alt rs886041081(A;A)
Reference Rs886041081(G;G)
Significance Pathogenic
Disease Mitochondrial DNA depletion syndrome 12a (cardiomyopathic type) not provided Mitochondrial diseases
Variation info
Gene SLC25A4
CLNDBN Mitochondrial DNA depletion syndrome 12a (cardiomyopathic type), autosomal dominant not provided Mitochondrial diseases
Reversed 0
HGVS NC_000004.11:g.186066045G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000258873.1, RCV000479591.1, RCV000491010.1,