Variants in gene TGFB2 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (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: 9

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HGVS	dbSNP	gnomAD frequency
NM_003238.6(TGFB2):c.274G>T (p.Glu92Ter)	rs1656706610
NM_003238.6(TGFB2):c.450_451del (p.Arg150fs)
NM_003238.6(TGFB2):c.821dup (p.Asn274fs)	rs863223796
NM_003238.6(TGFB2):c.895C>T (p.Arg299Trp)	rs863223792
NM_003238.6(TGFB2):c.896G>A (p.Arg299Gln)	rs1057521150
NM_003238.6(TGFB2):c.904C>T (p.Arg302Cys)	rs869312903
NM_003238.6(TGFB2):c.905G>A (p.Arg302His)	rs1553303213
NM_003238.6(TGFB2):c.933-1G>A
NM_003238.6(TGFB2):c.958C>T (p.Arg320Cys)	rs1553303352

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