Variant (rsID / SNP)

rs112276566

rs112276566 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC25A15. Location: chromosome 13, position 41,367,296. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SLC25A15Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 13:41367296
Cytoband: 13q14.11
HGVS: NM_014252.4(SLC25A15):c.-67A>T
Allele change: Silent

Associated conditions / phenotypes

Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

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.