ClinVar Miner

List of variants in gene DNM2 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 115
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001005361.3(DNM2):c.2059-136G>C rs8109524 0.01465
NM_001005361.3(DNM2):c.1671+283G>A rs60053169 0.01297
NM_001005361.3(DNM2):c.1557+193G>A rs146942869 0.01227
NM_001005361.3(DNM2):c.1493+252C>G rs117843888 0.01174
NM_001005361.3(DNM2):c.2291+153G>A rs113951641 0.01022
NM_001005361.3(DNM2):c.385+60A>G rs116398690 0.00931
NM_001005361.3(DNM2):c.1197-940A>G rs79068463 0.00917
NM_001005361.3(DNM2):c.161+248G>C rs75654370 0.00796
NM_001005361.3(DNM2):c.1336-196C>G rs180679346 0.00751
NM_001005361.3(DNM2):c.1197-242G>T rs115609558 0.00668
NM_001005361.3(DNM2):c.1335+324C>G rs115672648 0.00630
NM_001005361.3(DNM2):c.1336-82C>T rs148385341 0.00564
NM_001005361.3(DNM2):c.*47G>A rs367938944 0.00550
NM_001005361.3(DNM2):c.1672-337G>A rs75646078 0.00509
NM_001005361.3(DNM2):c.1557+63C>T rs114229076 0.00444
NM_001005361.3(DNM2):c.589+132T>C rs80295112 0.00360
NM_001005361.3(DNM2):c.589+139T>C rs142918508 0.00360
NM_001005361.3(DNM2):c.589+159C>T rs151092170 0.00359
NM_001005361.3(DNM2):c.589+86G>A rs146877273 0.00358
NM_001005361.3(DNM2):c.1128+241A>G rs56274124 0.00352
NM_001005361.3(DNM2):c.1558-213G>C rs191714992 0.00352
NM_001005361.3(DNM2):c.1545+14C>G rs114713494 0.00350
NM_001005361.3(DNM2):c.1196+158A>C rs186856304 0.00347
NM_001005361.3(DNM2):c.2544-235C>T rs139137394 0.00339
NM_001005361.3(DNM2):c.689-103C>T rs112762923 0.00314
NM_001005361.3(DNM2):c.1546-73C>T rs141100592 0.00276
NM_001005361.3(DNM2):c.850-53C>T rs527643558 0.00265
NM_001005361.3(DNM2):c.1781+17C>A rs75344643 0.00220
NM_001005361.3(DNM2):c.1782-5C>T rs200103145 0.00113
NM_001005361.3(DNM2):c.2061G>A (p.Thr687=) rs149164657 0.00102
NM_001005361.3(DNM2):c.589+17G>T rs374377836 0.00028
NM_001005361.3(DNM2):c.645C>T (p.Asp215=) rs148900299 0.00028
NM_001005361.3(DNM2):c.2511G>A (p.Arg837=) rs200100669 0.00027
NM_001005361.3(DNM2):c.958G>A (p.Asp320Asn) rs150613209 0.00026
NM_001005361.3(DNM2):c.1546-16C>T rs375554484 0.00022
NM_001005361.3(DNM2):c.1893+18G>A rs368748557 0.00022
NM_001005361.3(DNM2):c.882G>A (p.Pro294=) rs144790170 0.00018
NM_001005361.3(DNM2):c.480C>T (p.Ile160=) rs140036663 0.00017
NM_001005361.3(DNM2):c.1423-12G>A rs376753915 0.00014
NM_001005361.3(DNM2):c.789G>A (p.Pro263=) rs199976453 0.00014
NM_001005361.3(DNM2):c.822G>A (p.Thr274=) rs201763720 0.00014
NM_001005361.3(DNM2):c.1827C>T (p.Ser609=) rs371412466 0.00013
NM_001005361.3(DNM2):c.1422+9C>T rs199952853 0.00012
NM_001005361.3(DNM2):c.957C>T (p.Pro319=) rs141911457 0.00012
NM_001005361.3(DNM2):c.2592C>T (p.Ala864=) rs373161548 0.00011
NM_001005361.3(DNM2):c.*14C>T rs369529119 0.00010
NM_001005361.3(DNM2):c.2253T>C (p.Pro751=) rs200155565 0.00009
NM_001005361.3(DNM2):c.2313G>A (p.Pro771=) rs147463138 0.00009
NM_001005361.3(DNM2):c.315C>T (p.Thr105=) rs111837150 0.00009
NM_001005361.3(DNM2):c.555C>T (p.Asp185=) rs140788791 0.00009
NM_001005361.3(DNM2):c.633C>T (p.Asp211=) rs200191870 0.00009
NM_001005361.3(DNM2):c.666C>T (p.Asn222=) rs2229921 0.00008
NM_001005361.3(DNM2):c.876G>A (p.Ser292=) rs749140605 0.00008
NM_001005361.3(DNM2):c.1196+778G>C rs763908447 0.00006
NM_001005361.3(DNM2):c.1437C>T (p.Ile479=) rs146506201 0.00006
NM_001005361.3(DNM2):c.1449G>A (p.Gln483=) rs750299400 0.00006
NM_001005361.3(DNM2):c.1782-4G>A rs767424969 0.00006
NM_001005361.3(DNM2):c.1893+10C>T rs147321173 0.00006
NM_001005361.3(DNM2):c.2231T>C (p.Val744Ala) rs777609224 0.00006
NM_001005361.3(DNM2):c.312G>A (p.Glu104=) rs144970326 0.00006
NM_001005361.3(DNM2):c.450A>G (p.Pro150=) rs766121627 0.00006
NM_001005361.3(DNM2):c.1032C>T (p.Ile344=) rs747050783 0.00004
NM_001005361.3(DNM2):c.162-16T>C rs573469750 0.00004
NM_001005361.3(DNM2):c.1893+17C>T rs45585238 0.00004
NM_001005361.3(DNM2):c.2292-15T>A rs534518685 0.00004
NM_001005361.3(DNM2):c.2418G>A (p.Ala806=) rs200968756 0.00004
NM_001005361.3(DNM2):c.993-14C>T rs761380478 0.00004
NM_001005361.3(DNM2):c.1518G>C (p.Leu506=) rs201426481 0.00003
NM_001005361.3(DNM2):c.2016C>T (p.Arg672=) rs368131004 0.00003
NM_001005361.3(DNM2):c.2031G>A (p.Lys677=) rs768285660 0.00003
NM_001005361.3(DNM2):c.471G>A (p.Lys157=) rs757708760 0.00003
NM_001005361.3(DNM2):c.992+11C>T rs761511769 0.00003
NM_001005361.3(DNM2):c.162-12C>T rs746299224 0.00002
NM_001005361.3(DNM2):c.1836C>T (p.Asp612=) rs767061986 0.00002
NM_001005361.3(DNM2):c.1071C>T (p.Ser357=) rs779241319 0.00001
NM_001005361.3(DNM2):c.1128+13G>A rs772437963 0.00001
NM_001005361.3(DNM2):c.1423-13C>T rs771343870 0.00001
NM_001005361.3(DNM2):c.1423-4C>T rs552776205 0.00001
NM_001005361.3(DNM2):c.1494-19G>T rs1032876620 0.00001
NM_001005361.3(DNM2):c.1512G>A (p.Thr504=) rs767407905 0.00001
NM_001005361.3(DNM2):c.162-6del rs766449694 0.00001
NM_001005361.3(DNM2):c.1758C>T (p.Phe586=) rs766274376 0.00001
NM_001005361.3(DNM2):c.183A>G (p.Ser61=) rs149555942 0.00001
NM_001005361.3(DNM2):c.1872C>T (p.Gly624=) rs774256221 0.00001
NM_001005361.3(DNM2):c.1894-9C>T rs377410182 0.00001
NM_001005361.3(DNM2):c.243C>T (p.Ala81=) rs755366581 0.00001
NM_001005361.3(DNM2):c.2544-19G>A rs769617279 0.00001
NM_001005361.3(DNM2):c.402C>T (p.Leu134=) rs748069348 0.00001
NM_001005361.3(DNM2):c.654C>T (p.Asp218=) rs763948283 0.00001
NM_001005361.3(DNM2):c.858C>G (p.Thr286=) rs542637338 0.00001
NM_001005361.3(DNM2):c.1196+643C>T rs563985581
NM_001005361.3(DNM2):c.1336-258TGCCTCC[3] rs528685725
NM_001005361.3(DNM2):c.1493+16G>A rs1446097383
NM_001005361.3(DNM2):c.1545+11C>T rs1555712626
NM_001005361.3(DNM2):c.1546-18A>C rs1426762153
NM_001005361.3(DNM2):c.1557+9A>T rs778469445
NM_001005361.3(DNM2):c.1584C>T (p.Ile528=) rs935512495
NM_001005361.3(DNM2):c.162-7C>T rs148318860
NM_001005361.3(DNM2):c.162-9C>G rs200736669
NM_001005361.3(DNM2):c.1665T>C (p.Asp555=) rs1555713814
NM_001005361.3(DNM2):c.1671+325G>T rs147796686
NM_001005361.3(DNM2):c.1781+71CACTGAG[3] rs142612564
NM_001005361.3(DNM2):c.1782-4G>C rs767424969
NM_001005361.3(DNM2):c.1782-5del rs760441017
NM_001005361.3(DNM2):c.1782-5dup rs760441017
NM_001005361.3(DNM2):c.1782-7C>A rs200843089
NM_001005361.3(DNM2):c.2058+292A>C rs576987452
NM_001005361.3(DNM2):c.2256C>G (p.Val752=) rs751020224
NM_001005361.3(DNM2):c.2269C>A (p.Leu757Ile) rs375820696
NM_001005361.3(DNM2):c.235+12C>T rs147026993
NM_001005361.3(DNM2):c.2543+140G>T rs190422103
NM_001005361.3(DNM2):c.589+274C>G rs111624191
NM_001005361.3(DNM2):c.589+274C>T rs111624191
NM_001005361.3(DNM2):c.688+15del rs1555706470
NM_001005361.3(DNM2):c.831G>A (p.Leu277=) rs1555707690

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.