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Variant (rsID / SNP)

rs2306120

ACBD3

rs2306120 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACBD3. Location: chromosome 1, position 226,352,498. The table records no clinical significance for this variant.

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Reference-table entries

ACBD3Not classified
Variant type
missense_variant
Chromosome / position
1:226352498
HGVS
NM_022735.4,c.561A>C,p.Glu187Asp
Allele change
Missense_E187D

Public references

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