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Variant (rsID / SNP)

rs2074051

ACCSL

rs2074051 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACCSL. Location: chromosome 11, position 44,080,210. The table records no clinical significance for this variant.

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Reference-table entries

ACCSLNot classified
Variant type
missense_variant
Chromosome / position
11:44080210
HGVS
NM_001031854.2,c.1585T>C,p.Cys529Arg
Allele change
Missense_C348R

Public references

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