"SCARB1-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1181016	NM_005505.5(SCARB1):c.*72G>A	SCARB1	Single nucleotide variant (synonymous variant +2 more)	SCARB1-related condition +1 more	GBenign
Select item 3045145	NM_005505.5(SCARB1):c.*15C>T	SCARB1	Single nucleotide variant (synonymous variant +2 more)	SCARB1-related condition	GLikely benign
Select item 3057962	NM_005505.5(SCARB1):c.1255-10G>A	SCARB1	Single nucleotide variant (intron variant)	SCARB1-related condition	GLikely benign
Select item 1270257	NM_005505.5(SCARB1):c.1129-7G>A	LOC129390586, SCARB1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1236346	NM_005505.5(SCARB1):c.1050T>C (p.Ala350=)	SCARB1	Single nucleotide variant (synonymous variant +2 more)	SCARB1-related condition +1 more	GBenign
Select item 3014020	NM_005505.5(SCARB1):c.1008C>T (p.Phe336=)	SCARB1	Single nucleotide variant (synonymous variant +2 more)	SCARB1-related condition +1 more	GLikely benign
Select item 2071472	NM_005505.5(SCARB1):c.991G>A (p.Val331Ile)	SCARB1 (V323I +2 more)	Single nucleotide variant (missense variant +2 more)	SCARB1-related condition +1 more	GLikely benign
Select item 2075612	NM_005505.5(SCARB1):c.933G>A (p.Gly311=)	SCARB1	Single nucleotide variant (synonymous variant +2 more)	SCARB1-related condition +1 more	GBenign/Likely benign
Select item 1601376	NM_005505.5(SCARB1):c.631-14T>G	SCARB1	Single nucleotide variant (intron variant)	SCARB1-related condition +1 more	GBenign/Likely benign
Select item 1283188	NM_005505.5(SCARB1):c.501C>T (p.Gly167=)	SCARB1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 2770657	NM_005505.5(SCARB1):c.228C>T (p.Ser76=)	SCARB1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 2733662	NM_005505.5(SCARB1):c.126+4G>A	LOC130009157, SCARB1	Single nucleotide variant (intron variant)	SCARB1-related condition +1 more	GConflicting classifications of pathogenicity
Select item 788443	NM_005505.5(SCARB1):c.63C>T (p.Cys21=)	LOC130009157, SCARB1	Single nucleotide variant (synonymous variant +1 more)	SCARB1-related condition +1 more	GBenign/Likely benign
Select item 1283556	NM_005505.5(SCARB1):c.12C>T (p.Ser4=)	LOC130009157, SCARB1	Single nucleotide variant (synonymous variant +1 more)	SCARB1-related condition +1 more	GBenign