Variant (rsID / SNP)

rs8572

rs8572 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OXA1L. Location: chromosome 14, position 23,236,524. The table records no clinical significance for this variant.

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Reference-table entries

OXA1LNot classified

Variant type: missense_variant
Chromosome / position: 14:23236524
HGVS: NM_005015.5,c.131C>T,p.Ala44Val
Allele change: Missense_A104V

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.