List of variants in gene DIS3L2 reported as likely benign by Illumina Laboratory Services, Illumina

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_152383.5(DIS3L2):c.*558T>C	rs143549263	0.01498
NM_152383.5(DIS3L2):c.702+10T>G	rs184764939	0.00343
NM_152383.5(DIS3L2):c.-78C>T	rs114491317	0.00288
NM_152383.5(DIS3L2):c.2370C>T (p.Gly790=)	rs199541622	0.00242
NM_152383.5(DIS3L2):c.263C>T (p.Pro88Leu)	rs202059499	0.00073
NM_152383.5(DIS3L2):c.1317+15C>G	rs553691050	0.00001
NM_152383.5(DIS3L2):c.*86del	rs373401005

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