Variant (rsID / SNP)

rs183130

rs183130 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CETP. Location: chromosome 16, position 56,991,363. Clinical significance in the table: association.

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Reference-table entries

CETPAssociation

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 16:56991363
Cytoband: 16q13
HGVS: NG_008952.1:g.529C=

Associated conditions / phenotypes

High density lipoprotein cholesterol level quantitative trait locus 10

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.