ITGB3BP[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2477376	NM_014288.5(ITGB3BP):c.491G>C (p.Arg164Pro)	ITGB3BP (R164P +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2614411	NM_014288.5(ITGB3BP):c.439A>G (p.Asn147Asp)	ITGB3BP (N186D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3111444	NM_014288.5(ITGB3BP):c.433A>G (p.Lys145Glu)	ITGB3BP (K105E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3111443	NM_014288.5(ITGB3BP):c.381T>G (p.Cys127Trp)	ITGB3BP (C166W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208310	NM_014288.5(ITGB3BP):c.328A>G (p.Ile110Val)	ITGB3BP (I110V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368931	NM_014288.5(ITGB3BP):c.259A>G (p.Met87Val)	ITGB3BP (M47V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618910	NM_014288.5(ITGB3BP):c.255A>G (p.Glu85=)	ITGB3BP	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign

ClinVar