Variant (rsID / SNP)

rs11549081

rs11549081 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AACS. Location: chromosome 12, position 125,561,151. The table records no clinical significance for this variant.

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Reference-table entries

AACSNot classified

Variant type: missense_variant
Chromosome / position: 12:125561151
HGVS: NM_023928.5,c.352A>G,p.Ile118Val
Allele change: Missense_I118V

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.