"Birmingham Platelet Group; University of Birmingham"[submitter] AND " - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 695335	NM_000212.3(ITGB3):c.197T>G (p.Leu66Arg)	ITGB3 (L66R)	Single nucleotide variant (missense variant)	Glanzmann thrombasthenia	GBenign FDA Recognized database
Select item 988836	NM_000212.3(ITGB3):c.349C>T (p.Arg117Trp)	ITGB3 (R117W)	Single nucleotide variant (missense variant)	Abnormal bleeding +1 more	GLikely pathogenic