ClinVar Miner

List of variants in gene DIS3L2 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 82
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_152383.5(DIS3L2):c.211-131T>G rs896990 0.81469
NM_152383.5(DIS3L2):c.211-311A>G rs3116228 0.78735
NM_152383.5(DIS3L2):c.1124+269A>T rs723317 0.75425
NM_152383.5(DIS3L2):c.951-99A>G rs3116181 0.47692
NM_001257281.2(DIS3L2):c.*249T>C rs6711186 0.36155
NM_152383.5(DIS3L2):c.2496+265A>G rs9678004 0.14340
NM_152383.5(DIS3L2):c.2289+37G>A rs1814893 0.13403
NM_152383.5(DIS3L2):c.2646A>G (p.Ser882=) rs3811578 0.13184
NM_152383.5(DIS3L2):c.2159-168C>T rs3748966 0.11979
NM_152383.5(DIS3L2):c.456A>G (p.Gln152=) rs11887184 0.11049
NM_152383.5(DIS3L2):c.1426-195A>T rs16828734 0.09132
NM_152383.5(DIS3L2):c.34C>T (p.Pro12Ser) rs723044 0.07683
NM_152383.5(DIS3L2):c.1318-349A>G rs76648839 0.07527
NM_152383.5(DIS3L2):c.2011-177G>A rs3748967 0.06184
NM_152383.5(DIS3L2):c.950+242A>G rs79410303 0.05823
NM_152383.5(DIS3L2):c.2394+39C>T rs149870557 0.05650
NM_152383.5(DIS3L2):c.*103A>G rs113002914 0.04858
NM_152383.5(DIS3L2):c.2187C>T (p.Pro729=) rs75782436 0.04483
NM_152383.5(DIS3L2):c.1660-182A>G rs7595451 0.02952
NM_152383.5(DIS3L2):c.2394+141G>A rs545668540 0.02571
NM_152383.5(DIS3L2):c.1317+234A>G rs80029169 0.02101
NM_152383.5(DIS3L2):c.703-63C>T rs16828636 0.02069
NM_152383.5(DIS3L2):c.1170C>T (p.Leu390=) rs17272089 0.01655
NM_152383.5(DIS3L2):c.702+33A>G rs75061164 0.01611
NM_152383.5(DIS3L2):c.264+283G>A rs114010499 0.01252
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.265-15C>A rs114804860 0.01092
NM_152383.5(DIS3L2):c.*113T>G rs116379923 0.01035
NM_001257281.2(DIS3L2):c.*3A>C rs143390659 0.00811
NM_152383.5(DIS3L2):c.1448G>A (p.Arg483Gln) rs148474013 0.00804
NM_152383.5(DIS3L2):c.*315G>C rs192296021 0.00582
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.*255C>T rs143054885 0.00130
NM_152383.5(DIS3L2):c.878C>A (p.Pro293His) rs187563594 0.00121
NM_152383.5(DIS3L2):c.*77G>T rs77517611 0.00113
NM_152383.5(DIS3L2):c.1447C>G (p.Arg483Gly) rs186865544 0.00073
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.662C>G (p.Thr221Arg) rs201020526 0.00052
NM_152383.5(DIS3L2):c.795C>T (p.Tyr265=) rs202042951 0.00047
NM_152383.5(DIS3L2):c.1722G>T (p.Glu574Asp) rs191608083 0.00041
NM_152383.5(DIS3L2):c.2010+20G>A rs374190053 0.00038
NM_152383.5(DIS3L2):c.951-20C>T rs201896227 0.00023
NM_152383.5(DIS3L2):c.1430T>G (p.Leu477Arg) rs201719374 0.00022
NM_152383.5(DIS3L2):c.1019A>G (p.Tyr340Cys) rs200027186 0.00021
NM_152383.5(DIS3L2):c.2409G>T (p.Arg803=) rs148106618 0.00014
NM_152383.5(DIS3L2):c.1597C>A (p.His533Asn) rs372209368 0.00013
NM_152383.5(DIS3L2):c.2329A>G (p.Ile777Val) rs2697798 0.00013
NM_152383.5(DIS3L2):c.1680G>A (p.Leu560=) rs377644356 0.00008
NM_152383.5(DIS3L2):c.2067C>T (p.Tyr689=) rs186340144 0.00007
NM_152383.5(DIS3L2):c.1839C>T (p.Pro613=) rs187677159 0.00006
NM_152383.5(DIS3L2):c.1300G>A (p.Val434Ile) rs758366698 0.00005
NM_152383.5(DIS3L2):c.2244C>T (p.Arg748=) rs745415974 0.00004
NM_152383.5(DIS3L2):c.1567G>A (p.Glu523Lys) rs745936781 0.00003
NM_152383.5(DIS3L2):c.1317+15C>G rs553691050 0.00001
NM_152383.5(DIS3L2):c.1585G>A (p.Val529Ile) rs773893129 0.00001
NM_152383.5(DIS3L2):c.871G>A (p.Ala291Thr) rs753115829 0.00001
NM_001257281.2(DIS3L2):c.*79G>A rs77750940
NM_001257281.2(DIS3L2):c.1582-193C>T rs3924438
NM_001257281.2(DIS3L2):c.1582-78C>G rs1125045
NM_001257281.2(DIS3L2):c.1651_1652insGGG (p.Glu550_Ala551insGly) rs141560952
NM_152383.5(DIS3L2):c.*314A>T rs187723884
NM_152383.5(DIS3L2):c.1087A>G (p.Ile363Val) rs540563766
NM_152383.5(DIS3L2):c.1253C>T (p.Pro418Leu) rs752820747
NM_152383.5(DIS3L2):c.1659+18dup rs1693773339
NM_152383.5(DIS3L2):c.1782C>G (p.Ala594=) rs765160562
NM_152383.5(DIS3L2):c.211-10dup rs767260895
NM_152383.5(DIS3L2):c.2158+8del
NM_152383.5(DIS3L2):c.2159-10dup
NM_152383.5(DIS3L2):c.2496+11del
NM_152383.5(DIS3L2):c.2496+9C>T rs573355704
NM_152383.5(DIS3L2):c.265-10del
NM_152383.5(DIS3L2):c.52+9del rs2106220830
NM_152383.5(DIS3L2):c.703-3del
NM_152383.5(DIS3L2):c.730T>C (p.Ser244Pro) rs2106355288
NM_152383.5(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.