Variants in gene TCN2 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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_000355.4(TCN2):c.89T>G (p.Leu30Arg)	rs116605132	0.00388
NM_000355.4(TCN2):c.877C>T (p.Leu293=)	rs45624233	0.00347
NM_000355.4(TCN2):c.360G>A (p.Arg120=)	rs115272037	0.00321
NM_000355.4(TCN2):c.280G>A (p.Gly94Ser)	rs11557600	0.00162
NM_000355.4(TCN2):c.623G>A (p.Arg208His)	rs150472705	0.00154
NM_000355.4(TCN2):c.138C>T (p.Ser46=)	rs143250551	0.00148
NM_000355.4(TCN2):c.428-4T>C	rs201408393	0.00134
NM_000355.4(TCN2):c.501C>T (p.His167=)	rs144652799	0.00024
NM_000355.4(TCN2):c.547G>A (p.Val183Met)	rs201925682	0.00011
NM_000355.4(TCN2):c.581-8A>G	rs7290898

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