Variants in gene ITGA2B with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000419.5(ITGA2B):c.1210+105A>G	rs992856733	0.00001
NM_000419.5(ITGA2B):c.1005_1013del (p.His335_Leu338delinsGln)	rs1598381654
NM_000419.5(ITGA2B):c.2150T>C (p.Leu717Pro)	rs2143447451
NM_000419.5(ITGA2B):c.2507G>C (p.Gly836Ala)	rs759664025
NM_000419.5(ITGA2B):c.476G>T (p.Gly159Val)	rs2048641442
NM_000419.5(ITGA2B):c.574+5G>A	rs1598383011
NM_000419.5(ITGA2B):c.59T>G (p.Leu20Arg)
NM_000419.5(ITGA2B):c.800G>A (p.Gly267Glu)	rs2048627164
NM_000419.5(ITGA2B):c.886G>A (p.Gly296Arg)	rs753264426
NM_000419.5(ITGA2B):c.889G>C (p.Ala297Pro)	rs531610168

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