"Illumina Laboratory Services, Illumina"[submitter] AND "LOC130061041" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 255534	NM_000212.3(ITGB3):c.-7G>C	ITGB3, LOC130061041	Single nucleotide variant (5 prime UTR variant)	not specified +1 more	GBenign
Select item 891898	NM_000212.3(ITGB3):c.16C>T (p.Arg6Trp)	ITGB3, LOC130061041 (R6W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 891899	NM_000212.3(ITGB3):c.19C>T (p.Pro7Ser)	ITGB3, LOC130061041 (P7S)	Single nucleotide variant (missense variant)	Glanzmann thrombasthenia	GUncertain significance

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