Variant (rsID / SNP)
rs2302126
rs2302126 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH6A1. Location: chromosome 14, position 74,539,325. Clinical significance in the table: Benign.
Reference-table entries
ALDH6A1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:74539325
- Cytoband
- 14q24.3
- HGVS
- NM_005589.4(ALDH6A1):c.112-11G>T
- Allele change
- Silent
Associated conditions / phenotypes
Methylmalonate semialdehyde dehydrogenase deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.