ClinVar Miner

List of variants in gene DNA2 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_001080449.3(DNA2):c.1058-115G>A rs116034545 0.00931
NM_001080449.3(DNA2):c.939+81G>A rs7912091 0.00854
NM_001080449.3(DNA2):c.939+200C>T rs188115109 0.00735
NM_001080449.3(DNA2):c.442-130A>T rs146014341 0.00730
NM_001080449.3(DNA2):c.1058-306C>G rs144840488 0.00691
NM_001080449.3(DNA2):c.939+263A>G rs148286330 0.00690
NM_001080449.3(DNA2):c.442-39_442-38del rs200481479 0.00655
NM_001080449.3(DNA2):c.719+263G>A rs143432064 0.00655
NM_001080449.3(DNA2):c.588-238T>A rs147214403 0.00578
NM_001080449.3(DNA2):c.1983+285C>T rs115348257 0.00518
NM_001080449.3(DNA2):c.1221-245C>T rs77444626 0.00485
NM_001080449.3(DNA2):c.74+111C>A rs115640956 0.00430
NM_001080449.3(DNA2):c.2153G>T (p.Cys718Phe) rs147096750 0.00367
NM_001080449.3(DNA2):c.1415+59C>T rs550225061 0.00337
NM_001080449.3(DNA2):c.940-24G>A rs144413502 0.00207
NM_001080449.3(DNA2):c.1796G>A (p.Arg599His) rs201999986 0.00068
NM_001080449.3(DNA2):c.1476T>C (p.Cys492=) rs373089726 0.00051
NM_001080449.3(DNA2):c.2697+18T>C rs190301454 0.00040
NM_001080449.3(DNA2):c.2473G>A (p.Val825Met) rs201513130 0.00014
NM_001080449.3(DNA2):c.2826G>A (p.Pro942=) rs200956547 0.00011
NM_001080449.3(DNA2):c.-21T>G rs375303446 0.00010
NM_001080449.3(DNA2):c.264T>C (p.Ser88=) rs749078276 0.00009
NM_001080449.3(DNA2):c.2706G>A (p.Ala902=) rs371684850 0.00009
NM_001080449.3(DNA2):c.1763+14A>C rs544079864 0.00007
NM_001080449.3(DNA2):c.1116T>C (p.Ser372=) rs368778086 0.00003
NM_001080449.3(DNA2):c.2358G>A (p.Gly786=) rs773533815 0.00003
NM_001080449.3(DNA2):c.1415+16A>C rs751137634 0.00002
NM_001080449.3(DNA2):c.1719C>T (p.Thr573=) rs1295862594 0.00001
NM_001080449.3(DNA2):c.3087G>A (p.Leu1029=) rs754444650 0.00001
NM_001080449.3(DNA2):c.441+15C>T rs558303170 0.00001
NM_001080449.3(DNA2):c.*202del rs529121415
NM_001080449.3(DNA2):c.-48dup rs762749916
NM_001080449.3(DNA2):c.1057+16T>C rs1057521508
NM_001080449.3(DNA2):c.1058-13dup rs201474338
NM_001080449.3(DNA2):c.1416-11T>C rs1345473976
NM_001080449.3(DNA2):c.1416-242_1416-241insTTG rs1554905593
NM_001080449.3(DNA2):c.1416-246_1416-244dup rs764493127
NM_001080449.3(DNA2):c.1491A>G (p.Leu497=) rs549990947
NM_001080449.3(DNA2):c.1983+12A>C rs1057521699
NM_001080449.3(DNA2):c.2209-11C>T rs538970967
NM_001080449.3(DNA2):c.2430C>T (p.Phe810=) rs73274785
NM_001080449.3(DNA2):c.2697+13_2697+17delinsTT rs1064794608
NM_001080449.3(DNA2):c.64_74+1del rs556723627
NM_001080449.3(DNA2):c.719+62GT[2] rs140385668
NM_001080449.3(DNA2):c.720-15_720-14dup rs34191745
NM_001080449.3(DNA2):c.720-15dup rs34191745
NM_001080449.3(DNA2):c.720-84GT[2] rs150251397
NM_001080449.3(DNA2):c.74+13G>C rs370226465
NM_001080449.3(DNA2):c.940-331_940-317del rs200343842

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