List of variants in gene DIS3L2 reported as likely benign by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_152383.5(DIS3L2):c.2370C>T (p.Gly790=)	rs199541622	0.00242
NM_152383.5(DIS3L2):c.795C>T (p.Tyr265=)	rs202042951	0.00047
NM_152383.5(DIS3L2):c.360T>C (p.His120=)	rs748055073	0.00003
NM_152383.5(DIS3L2):c.288T>C (p.Ile96=)	rs746032745	0.00001
NM_152383.5(DIS3L2):c.*11CCGCCTGCC[4]	rs538186468
NM_152383.5(DIS3L2):c.2394+7G>A	rs372069869

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