List of variants in gene DIS3L2 reported as benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_152383.5(DIS3L2):c.2646A>G (p.Ser882=)	rs3811578	0.13184
NM_152383.5(DIS3L2):c.456A>G (p.Gln152=)	rs11887184	0.11049
NM_152383.5(DIS3L2):c.2187C>T (p.Pro729=)	rs75782436	0.04483
NM_152383.5(DIS3L2):c.1170C>T (p.Leu390=)	rs17272089	0.01655
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.1448G>A (p.Arg483Gln)	rs148474013	0.00804
NM_152383.5(DIS3L2):c.702+10T>G	rs184764939	0.00343

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