ClinVar Miner

List of variants in gene DNA2 reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_001080449.3(DNA2):c.2713C>A (p.Gln905Lys) rs181679245 0.00459
NM_001080449.3(DNA2):c.2697+18T>C rs190301454 0.00040
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.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.3087G>A (p.Leu1029=) rs754444650 0.00001
NM_001080449.3(DNA2):c.441+15C>T rs558303170 0.00001
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.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.2697+13_2697+17delinsTT rs1064794608
NM_001080449.3(DNA2):c.2698-20C>G
NM_001080449.3(DNA2):c.720-9T>G
NM_001080449.3(DNA2):c.74+12G>A
NM_001080449.3(DNA2):c.74+13G>C rs370226465
NM_001080449.3(DNA2):c.74+17dup

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