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Variant (rsID / SNP)

rs25683

ACAT2

rs25683 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACAT2. Location: chromosome 6, position 160,196,343. The table records no clinical significance for this variant.

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Reference-table entries

ACAT2Not classified
Variant type
missense_variant&splice_region_variant
Chromosome / position
6:160196343
HGVS
NM_001303253.1,c.719A>G,p.Lys240Arg
Allele change
Missense_K211R

Public references

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