Variants in gene ITGA2B with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_000419.5(ITGA2B):c.207C>T (p.Gly69=)	rs375882355	0.00038
NM_000419.5(ITGA2B):c.671-13C>T	rs200108644	0.00026
NM_000419.5(ITGA2B):c.1439+8C>T	rs371050454	0.00007
NM_000419.5(ITGA2B):c.891+12del	rs373578804

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