"CETP-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 319971	NM_000078.3(CETP):c.66C>A (p.Thr22=)	CETP	Single nucleotide variant (synonymous variant)	CETP-related condition +2 more	GBenign/Likely benign
Select item 885591	NM_000078.3(CETP):c.443G>A (p.Cys148Tyr)	CETP (C148Y)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 3042539	NM_000078.3(CETP):c.450T>C (p.Ser150=)	CETP	Single nucleotide variant (synonymous variant)	CETP-related condition	GLikely benign
Select item 785534	NM_000078.3(CETP):c.756T>C (p.His252=)	CETP	Single nucleotide variant (synonymous variant +1 more)	CETP-related condition +1 more	GBenign
Select item 721350	NM_000078.3(CETP):c.921C>T (p.Asp307=)	CETP	Single nucleotide variant (synonymous variant +1 more)	Hyperalphalipoproteinemia 1 +2 more	GBenign/Likely benign
Select item 319986	NM_000078.3(CETP):c.991G>A (p.Gly331Ser)	CETP (G331S +1 more)	Single nucleotide variant (missense variant)	Hyperalphalipoproteinemia 1 +2 more	GBenign/Likely benign
Select item 319989	NM_000078.3(CETP):c.1146+7C>T	CETP	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 319990	NM_000078.3(CETP):c.1153G>A (p.Val385Met)	CETP (V385M +1 more)	Single nucleotide variant (missense variant)	CETP-related condition +2 more	GBenign/Likely benign
Select item 319991	NM_000078.3(CETP):c.1161C>G (p.Thr387=)	CETP	Single nucleotide variant (synonymous variant)	CETP-related condition +2 more	GBenign
Select item 319997	NM_000078.3(CETP):c.1377C>T (p.Asp459=)	CETP	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign