Variant (rsID / SNP)
rs117824913
rs117824913 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OAT. Location: chromosome 10, position 126,107,465. Clinical significance in the table: Benign.
Reference-table entries
OATBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:126107465
- Cytoband
- 10q26.13
- HGVS
- NM_000274.4(OAT):c.-53C>T
- Allele change
- Silent
Associated conditions / phenotypes
Ornithine aminotransferase deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.