Variants in gene TSEN2 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (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_025265.4(TSEN2):c.909+34G>A	rs78943415	0.02811
NM_025265.4(TSEN2):c.1350G>A (p.Leu450=)	rs116627250	0.01389
NM_025265.4(TSEN2):c.-18+1G>T	rs147893483	0.00741
NM_025265.4(TSEN2):c.272-4C>G	rs41293385	0.00369
NM_025265.4(TSEN2):c.66A>C (p.Pro22=)	rs62637658	0.00322
NM_025265.4(TSEN2):c.1389C>T (p.Asp463=)	rs75288720	0.00287
NM_025265.4(TSEN2):c.405G>A (p.Pro135=)	rs140728375	0.00090
NM_025265.4(TSEN2):c.870A>G (p.Pro290=)	rs542708828	0.00006
NM_025265.4(TSEN2):c.389A>C (p.Lys130Thr)	rs142211875	0.00005
NM_025265.4(TSEN2):c.560G>C (p.Arg187Pro)	rs146117200

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