Variant (rsID / SNP)
rs887241
rs887241 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH3A1. Location: chromosome 17, position 19,645,938. The table records no clinical significance for this variant.
Reference-table entries
ALDH3A1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:19645938
- HGVS
- NM_000691.5,c.400T>G,p.Ser134Ala
- Allele change
- Missense_S134A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.