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

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 20

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HGVS	dbSNP	gnomAD frequency
NM_000419.5(ITGA2B):c.1787T>C (p.Ile596Thr)	rs76811038	0.00006
NM_000419.5(ITGA2B):c.2602-3C>G	rs763330792	0.00003
NM_000419.5(ITGA2B):c.1186G>A (p.Asp396Asn)	rs1214448436	0.00001
NM_000419.5(ITGA2B):c.1361G>A (p.Gly454Asp)	rs2048591163	0.00001
NM_000419.5(ITGA2B):c.1946+1G>A	rs746091910	0.00001
NM_000419.5(ITGA2B):c.2333A>C (p.Gln778Pro)	rs74475415	0.00001
NM_000419.5(ITGA2B):c.526C>G (p.Pro176Ala)	rs2048640485	0.00001
NM_000419.5(ITGA2B):c.1234G>A (p.Gly412Arg)	rs780786843
NM_000419.5(ITGA2B):c.1346G>A (p.Gly449Asp)	rs1598380253
NM_000419.5(ITGA2B):c.1366_1371del (p.Val456_Asp457del)	rs780017389
NM_000419.5(ITGA2B):c.138dup (p.Gly47fs)	rs2143506473
NM_000419.5(ITGA2B):c.2344C>T (p.Arg782Ter)	rs1598377051
NM_000419.5(ITGA2B):c.2444A>G (p.Tyr815Cys)	rs2048541187
NM_000419.5(ITGA2B):c.2930del (p.Arg977fs)	rs2048523431
NM_000419.5(ITGA2B):c.2965del (p.Ala989fs)	rs2048521625
NM_000419.5(ITGA2B):c.3076C>T (p.Arg1026Trp)	rs766503255
NM_000419.5(ITGA2B):c.3077G>A (p.Arg1026Gln)	rs879255514
NM_000419.5(ITGA2B):c.559del (p.Val187fs)	rs1469711487
NM_000419.5(ITGA2B):c.818G>A (p.Gly273Asp)	rs137852907
NM_000419.5(ITGA2B):c.998+1G>C	rs1598381778

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