List of variants in gene CETP reported as uncertain significance by GeneDx

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000078.3(CETP):c.1376A>G (p.Asp459Gly)	rs2303790	0.00102
NM_000078.3(CETP):c.1456G>A (p.Val486Met)	rs5887	0.00054
NM_000078.3(CETP):c.316G>A (p.Val106Met)	rs371258270	0.00019
NM_000078.3(CETP):c.869T>C (p.Leu290Pro)	rs369941536	0.00015
NM_000078.3(CETP):c.89G>A (p.Cys30Tyr)	rs771585518	0.00007
NM_000078.3(CETP):c.1022A>G (p.His341Arg)	rs762315471	0.00006
NM_000078.3(CETP):c.1105C>T (p.Arg369Cys)	rs774433762	0.00004
NM_000078.3(CETP):c.1159A>G (p.Thr387Ala)
NM_000078.3(CETP):c.1294G>A (p.Ala432Thr)	rs2056193601
NM_000078.3(CETP):c.443G>A (p.Cys148Tyr)	rs778814831

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