Variant (rsID / SNP)

rs13197086

rs13197086 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH5A1. Location: chromosome 6, position 24,536,706. Clinical significance in the table: Benign.

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Reference-table entries

ALDH5A1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:24536706
Cytoband: 6p22.3
HGVS: NM_001080.3(ALDH5A1):c.*2766G>A
Allele change: Silent

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.