List of variants in gene combination ITGB3, LOC130061043 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.662C>T (p.Thr221Met)	rs770992614	0.00003
NM_000212.3(ITGB3):c.652C>T (p.His218Tyr)	rs2143096777

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