Variant (rsID / SNP)

rs41294808

rs41294808 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACOT11. Location: chromosome 1, position 55,050,353. The table records no clinical significance for this variant.

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Reference-table entries

ACOT11Not classified

Variant type: missense_variant
Chromosome / position: 1:55050353
HGVS: NM_015547.4,c.59G>A,p.Arg20His
Allele change: Missense_R20H

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.