Variant (rsID / SNP)

rs727503795

rs727503795 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACAT1. Location: chromosome 11, position 108,009,633. Clinical significance in the table: Pathogenic/Likely pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ACAT1Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: Deletion
Chromosome / position: 11:108009633
Cytoband: 11q22.3
HGVS: NM_000019.4(ACAT1):c.444_445del (p.Met148fs)

Associated conditions / phenotypes

Deficiency of acetyl-CoA acetyltransferase

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.