Variants in gene TNXB 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001365276.2(TNXB):c.2030A>G (p.Asp677Gly)	rs141190850	0.00158
NM_001365276.2(TNXB):c.5103C>A (p.Phe1701Leu)	rs201360247	0.00058
NM_001365276.2(TNXB):c.6074A>T (p.Asp2025Val)	rs201397168	0.00055
NM_001365276.2(TNXB):c.9661G>A (p.Val3221Met)	rs367685759	0.00019
NM_001365276.2(TNXB):c.8542G>C (p.Gly2848Arg)	rs61745355

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