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Variant (rsID / SNP)

rs1554005

ACOXL

rs1554005 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACOXL. Location: chromosome 2, position 111,598,958. The table records no clinical significance for this variant.

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Reference-table entries

ACOXLNot classified
Variant type
missense_variant
Chromosome / position
2:111598958
HGVS
NM_001142807.4,c.764C>T,p.Thr255Met
Allele change
Missense_T255M

Public references

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