Variant (rsID / SNP)

rs1800777

rs1800777 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CETP. Location: chromosome 16, position 57,017,319. Clinical significance in the table: Benign.

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Reference-table entries

CETPBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:57017319
Cytoband: 16q13
HGVS: NM_000078.3(CETP):c.1403G>A (p.Arg468Gln)
Allele change: Missense_R408Q

Associated conditions / phenotypes

Hyperalphalipoproteinemia 1

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.