Variant (rsID / SNP)

rs2271738

rs2271738 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGO2. Location: chromosome 8, position 141,566,311. The table records no clinical significance for this variant.

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Reference-table entries

AGO2Not classified

Variant type: synonymous_variant
Chromosome / position: 8:141566311
HGVS: NM_012154.5,c.1101G>A,p.Ala367Ala
Allele change: Synonymous_A367A

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.