Variant (rsID / SNP)

rs146159281

rs146159281 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC25A26. Location: chromosome 3, position 66,287,056. Clinical significance in the table: Benign.

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Reference-table entries

SLC25A26Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:66287056
Cytoband: 3p14.1
HGVS: NM_001379210.1(SLC25A26):c.122G>A (p.Ser41Asn)
Allele change: Missense_S41N

Associated conditions / phenotypes

Combined oxidative phosphorylation deficiency 28

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.