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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000355.4(TCN2):c.138C>T (p.Ser46=)	rs143250551	0.00148
NM_000355.4(TCN2):c.296A>C (p.Lys99Thr)	rs150225103	0.00135
NM_000355.4(TCN2):c.428-4T>C	rs201408393	0.00134
NM_000355.4(TCN2):c.523G>A (p.Val175Met)	rs142791153	0.00134
NM_000355.4(TCN2):c.784G>C (p.Glu262Gln)	rs61743653	0.00056
NM_000355.4(TCN2):c.903C>T (p.Tyr301=)	rs146036025	0.00026
NM_000355.4(TCN2):c.522C>T (p.Ser174=)	rs537115632	0.00021
NM_000355.4(TCN2):c.1017C>G (p.Leu339=)	rs35997415	0.00019
NM_000355.4(TCN2):c.921A>C (p.Pro307=)	rs138738105	0.00010
NM_000355.4(TCN2):c.424A>G (p.Ile142Val)	rs200771616	0.00008
NM_000355.4(TCN2):c.882C>T (p.Pro294=)	rs142689742	0.00003
NM_000355.4(TCN2):c.459C>T (p.Ser153=)	rs201344377	0.00001
NM_000355.4(TCN2):c.1092G>A (p.Glu364=)	rs886057397
NM_000355.4(TCN2):c.581-8A>G	rs7290898
NM_000355.4(TCN2):c.810G>T (p.Ala270=)	rs61748898

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