Variants in gene DIS3L2 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_152383.5(DIS3L2):c.1488T>C (p.His496=)	rs72998118	0.01233
NM_152383.5(DIS3L2):c.426C>T (p.Pro142=)	rs73001172	0.01166
NM_152383.5(DIS3L2):c.702+10T>G	rs184764939	0.00343
NM_152383.5(DIS3L2):c.*13G>A	rs200467865	0.00304
NM_152383.5(DIS3L2):c.702+39T>G	rs75968600	0.00289
NM_152383.5(DIS3L2):c.2370C>T (p.Gly790=)	rs199541622	0.00242
NM_152383.5(DIS3L2):c.1570G>A (p.Glu524Lys)	rs201308521	0.00147
NM_152383.5(DIS3L2):c.878C>A (p.Pro293His)	rs187563594	0.00121
NM_152383.5(DIS3L2):c.263C>T (p.Pro88Leu)	rs202059499	0.00073
NM_152383.5(DIS3L2):c.1911A>C (p.Ala637=)	rs563679311	0.00072
NM_152383.5(DIS3L2):c.410A>G (p.Tyr137Cys)	rs201733073	0.00072
NM_152383.5(DIS3L2):c.2067C>T (p.Tyr689=)	rs186340144	0.00007
NM_152383.5(DIS3L2):c.1317+15C>G	rs553691050	0.00001
NM_152383.5(DIS3L2):c.874C>A (p.Arg292=)	rs182004457

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