Variant (rsID / SNP)

rs62621664

rs62621664 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH5A1. Location: chromosome 6, position 24,505,196. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ALDH5A1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:24505196
Cytoband: 6p22.3
HGVS: NM_001080.3(ALDH5A1):c.709G>T (p.Ala237Ser)
Allele change: Missense_A237S

Associated conditions / phenotypes

Succinate-semialdehyde dehydrogenase deficiency

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.