Variant (rsID / SNP)

rs4420638

rs4420638 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOC1. Location: chromosome 19, position 45,422,946. The table records no clinical significance for this variant.

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Reference-table entries

APOC1Not classified

Variant type: single nucleotide variant
Chromosome / position: 19:45422946
Cytoband: 19q13.32
HGVS: NM_001645.3(APOC1):c.*459A>G

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.