Variant (rsID / SNP)
rs6695033
rs6695033 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH4A1. Location: chromosome 1, position 19,201,919. Clinical significance in the table: Benign.
Reference-table entries
ALDH4A1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:19201919
- Cytoband
- 1p36.13
- HGVS
- NM_003748.4(ALDH4A1):c.1417A>G (p.Thr473Ala)
- Allele change
- Missense_T473A
Associated conditions / phenotypes
Deficiency of pyrroline-5-carboxylate reductase
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.