List of variants in gene combination ITGB3, LOC130061045 reported as uncertain significance for hematologic disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000212.3(ITGB3):c.836A>T (p.Lys279Met)	rs79775494	0.00001
NM_000212.3(ITGB3):c.856G>C (p.Gly286Arg)	rs1199275720

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