Variant (rsID / SNP)

rs5167

rs5167 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOC4, APOC2. Location: chromosome 19, position 45,448,465. The table records no clinical significance for this variant.

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Reference-table entries

APOC4Not classified

Variant type: missense_variant
Chromosome / position: 19:45448465
HGVS: NM_001646.3,c.287T>G,p.Leu96Arg
Allele change: Missense_L96R

Associated conditions / phenotypes

Lipoprotein Quantitative Trait Locus|Hypercholesterolemia, Familial, 1|Arteries, Anomalies of|Hypercholesterolemia, Familial, 3

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.