Variant (rsID / SNP)

rs34607174

rs34607174 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACOT12. Location: chromosome 5, position 80,641,789. The table records no clinical significance for this variant.

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Reference-table entries

ACOT12Not classified

Variant type: missense_variant
Chromosome / position: 5:80641789
HGVS: NM_130767.3,c.688G>A,p.Val230Ile
Allele change: Silent

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.