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Variant (rsID / SNP)

rs1143659

ALDH9A1

rs1143659 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH9A1. Location: chromosome 1, position 165,652,273. The table records no clinical significance for this variant.

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Reference-table entries

ALDH9A1Not classified
Variant type
synonymous_variant
Chromosome / position
1:165652273
HGVS
NM_000696.4,c.402T>C,p.Ile134Ile
Allele change
Synonymous_I134I

Public references

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