Variant (rsID / SNP)
rs2072330
rs2072330 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH3A1. Location: chromosome 17, position 19,644,472. The table records no clinical significance for this variant.
Reference-table entries
ALDH3A1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:19644472
- HGVS
- NM_000691.5,c.741T>A,p.Pro247Pro
- Allele change
- Synonymous_P247P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
