ClinVar Miner

List of variants in gene LMNA reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP gnomAD frequency
NM_170707.4(LMNA):c.356+310T>C rs547915 0.79271
NM_170707.4(LMNA):c.514-197A>C rs569025 0.24095
NM_170707.4(LMNA):c.1338T>C (p.Asp446=) rs505058 0.23806
NM_170707.4(LMNA):c.1380+142G>A rs476000 0.23543
NM_170707.4(LMNA):c.1699-231T>C rs520910 0.23512
NM_170707.4(LMNA):c.357-3991T>G rs594028 0.22050
NM_170707.4(LMNA):c.357-4696T>C rs2485674 0.22050
NM_170707.4(LMNA):c.1698C>T (p.His566=) rs4641 0.20715
NM_170707.4(LMNA):c.861T>C (p.Ala287=) rs538089 0.18331
NM_170707.4(LMNA):c.1157+16G>A rs534807 0.18318
NM_170707.4(LMNA):c.1699-260C>T rs520973 0.17755
NM_170707.4(LMNA):c.1489-41C>T rs553016 0.17380
NM_170707.4(LMNA):c.936+234C>T rs2485664 0.17175
NM_170707.4(LMNA):c.357-778C>G rs665979 0.12915
NM_170707.4(LMNA):c.357-4760T>C rs2485675 0.10858
NM_170707.4(LMNA):c.357-4652C>T rs2485673 0.10835
NM_170707.4(LMNA):c.357-4560C>T rs2475758 0.10831
NM_170707.4(LMNA):c.357-4599C>A rs2485672 0.10819
NM_170707.4(LMNA):c.357-3535T>C rs622834 0.10805
NM_170707.4(LMNA):c.357-4021G>A rs593987 0.10778
NM_170707.4(LMNA):c.357-3489G>A rs623189 0.08469
NM_170707.4(LMNA):c.639+56G>T rs11264442 0.07070
NM_170707.4(LMNA):c.639+73C>T rs11264443 0.06637
NM_170707.4(LMNA):c.1608+143A>G rs41310120 0.05855
NM_170707.4(LMNA):c.937-275A>G rs76017998 0.05847
NM_170707.4(LMNA):c.*365C>T rs74116489 0.05784
NM_170707.4(LMNA):c.810+61C>T rs11264445 0.05733
NM_170707.4(LMNA):c.357-4032G>A rs6657367 0.05460
NM_170707.4(LMNA):c.810+13G>T rs11264444 0.05317
NM_170707.4(LMNA):c.1968+26A>G rs80264244 0.03826
NM_170707.4(LMNA):c.*393T>C rs111601180 0.03807
NM_170707.4(LMNA):c.514-111C>T rs78499673 0.02565
NM_170707.4(LMNA):c.1609-108G>A rs114316250 0.02419
NC_000001.11:g.156140128C>T rs570070 0.02418
NM_170707.4(LMNA):c.1158-43A>G rs16837198 0.02198
NM_170707.4(LMNA):c.1608+152A>G rs12058407 0.01802
NM_170707.4(LMNA):c.357-3431G>A rs76113322 0.01792
NM_170707.4(LMNA):c.1158-44C>T rs141879453 0.00929
NM_170707.4(LMNA):c.936+66C>T rs17847241 0.00670
NM_170707.4(LMNA):c.612G>A (p.Leu204=) rs12117552 0.00637
NM_170707.4(LMNA):c.*747G>A rs189656652 0.00611
NM_170707.4(LMNA):c.811-13T>A rs80356809 0.00309
NM_170707.4(LMNA):c.1761G>A (p.Leu587=) rs80356813 0.00210
NM_170707.4(LMNA):c.1851C>T (p.Ala617=) rs143189394 0.00158
NM_170707.4(LMNA):c.1566C>T (p.Cys522=) rs149339264 0.00123
NM_170707.4(LMNA):c.1489-16C>G rs201379016 0.00076
NM_170707.4(LMNA):c.1911C>T (p.Phe637=) rs117939448 0.00048
NM_170707.4(LMNA):c.789G>A (p.Leu263=) rs148557956 0.00048
NM_170707.4(LMNA):c.357-4426G>A rs540937543 0.00035
NM_170707.4(LMNA):c.1656C>T (p.Asp552=) rs370219874 0.00016
NM_170707.4(LMNA):c.1149G>A (p.Glu383=) rs267607603 0.00006
NM_170707.4(LMNA):c.1488G>A (p.Thr496=) rs375516745 0.00005
NM_170707.4(LMNA):c.-98G>C rs904723441 0.00004
NM_005572.4(LMNA):c.1712G>A (p.Arg571His) rs200917748 0.00003
NM_170707.4(LMNA):c.1381-13A>G rs750192865 0.00003
NM_170707.4(LMNA):c.1157+6C>G rs374768416 0.00002
NM_170707.4(LMNA):c.810+12C>T rs746914371 0.00002
NM_170707.4(LMNA):c.12G>A (p.Pro4=) rs369823958 0.00001
NM_170707.4(LMNA):c.870G>A (p.Glu290=) rs747275587 0.00001
NM_170707.4(LMNA):c.*192A>C rs708605
NM_170707.4(LMNA):c.*196_*197insA rs1651921286
NM_170707.4(LMNA):c.*211del rs200317083
NM_170707.4(LMNA):c.*211dup rs200317083
NM_170707.4(LMNA):c.*79G>C rs7339
NM_170707.4(LMNA):c.-147C>A rs1263529375
NM_170707.4(LMNA):c.-148C>A rs2102816121
NM_170707.4(LMNA):c.-88G>T rs115800510
NM_170707.4(LMNA):c.1551G>A (p.Gln517=) rs41314035
NM_170707.4(LMNA):c.1968+18dup rs554157057
NM_170707.4(LMNA):c.1968+20dup rs2102902744
NM_170707.4(LMNA):c.357-3588_357-3580del rs113124909
NM_170707.4(LMNA):c.357-4646AAT[3] rs150950685

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