ClinVar Miner

List of variants in gene DIS3L2 reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
NM_152383.4(DIS3L2):c.1019A>G (p.Tyr340Cys) rs200027186
NM_152383.4(DIS3L2):c.1170C>T (p.Leu390=) rs17272089
NM_152383.4(DIS3L2):c.1448G>A (p.Arg483Gln) rs148474013
NM_152383.4(DIS3L2):c.1488T>C (p.His496=) rs72998118
NM_152383.4(DIS3L2):c.1570G>A (p.Glu524Lys) rs201308521
NM_152383.4(DIS3L2):c.1680G>A (p.Leu560=) rs377644356
NM_152383.4(DIS3L2):c.1839C>T (p.Pro613=) rs187677159
NM_152383.4(DIS3L2):c.1911A>C (p.Ala637=) rs563679311
NM_152383.4(DIS3L2):c.2187C>T (p.Pro729=) rs75782436
NM_152383.4(DIS3L2):c.2370C>T (p.Gly790=) rs199541622
NM_152383.4(DIS3L2):c.263C>T (p.Pro88Leu) rs202059499
NM_152383.4(DIS3L2):c.34C>T (p.Pro12Ser) rs723044
NM_152383.4(DIS3L2):c.410A>G (p.Tyr137Cys) rs201733073
NM_152383.4(DIS3L2):c.426C>T (p.Pro142=) rs73001172
NM_152383.4(DIS3L2):c.702+10T>G rs184764939
NM_152383.4(DIS3L2):c.874C>A (p.Arg292=) rs182004457

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.