List of variants in gene ITGB3 reported as pathogenic by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000212.3(ITGB3):c.428T>G (p.Leu143Trp)	rs121918452	0.00002
NM_000212.3(ITGB3):c.725G>A (p.Arg242Gln)	rs377162158	0.00001
NM_000212.3(ITGB3):c.1402G>T (p.Glu468Ter)	rs2143112940
NM_000212.3(ITGB3):c.921C>A (p.Tyr307Ter)	rs2143099209

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