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Variant (rsID / SNP)

rs2271586

ART5

rs2271586 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ART5. Location: chromosome 11, position 3,659,993. The table records no clinical significance for this variant.

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Reference-table entries

ART5Not classified
Variant type
missense_variant
Chromosome / position
11:3659993
HGVS
NM_001079536.2,c.851C>A,p.Thr284Lys
Allele change
Missense_T284K

Public references

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