List of variants in gene CETP reported as likely pathogenic for hyperlipoproteinemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000078.3(CETP):c.1321+1G>A	rs5742907	0.00002
NM_000078.3(CETP):c.160C>T (p.Arg54Ter)	rs780627434
NM_000078.3(CETP):c.266del (p.Ser89fs)
NM_000078.3(CETP):c.964C>T (p.Gln322Ter)
NM_000078.3(CETP):c.981+2T>C	rs2142001776

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