Variant (rsID / SNP)

rs267606664

rs267606664 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOE. Location: chromosome 19, position 45,411,987. Clinical significance in the table: Uncertain significance.

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Reference-table entries

APOEUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 19:45411987
Cytoband: 19q13.32
HGVS: NM_000041.4(APOE):c.434G>A (p.Gly145Asp)
Allele change: Missense_G145D

Associated conditions / phenotypes

Hypercholesterolemia

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.