ClinVar Miner

List of variants in gene LMNA reported as benign for not provided

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Gene type:
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Total variants: 37
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HGVS dbSNP
NC_000001.11:g.156125971_156125973del
NM_005572.3(LMNA):c.1698C>T (p.His566=) rs4641
NM_170707.4(LMNA):c.1051A>C (p.Arg351=) rs771623461
NM_170707.4(LMNA):c.1158-43A>G rs16837198
NM_170707.4(LMNA):c.1158-44C>T rs141879453
NM_170707.4(LMNA):c.1338T>C (p.Asp446=) rs505058
NM_170707.4(LMNA):c.1380+142G>A
NM_170707.4(LMNA):c.1551G>A (p.Gln517=) rs41314035
NM_170707.4(LMNA):c.1608+152A>G
NM_170707.4(LMNA):c.1699-231T>C
NM_170707.4(LMNA):c.1699-260C>T
NM_170707.4(LMNA):c.1761G>A (p.Leu587=) rs80356813
NM_170707.4(LMNA):c.1968+26A>G rs80264244
NM_170707.4(LMNA):c.356+310T>C
NM_170707.4(LMNA):c.357-269T>C
NM_170707.4(LMNA):c.357-3489G>A
NM_170707.4(LMNA):c.357-3535T>C
NM_170707.4(LMNA):c.357-3991T>G
NM_170707.4(LMNA):c.357-4021G>A
NM_170707.4(LMNA):c.357-4032G>A
NM_170707.4(LMNA):c.357-4560C>T
NM_170707.4(LMNA):c.357-4652C>T
NM_170707.4(LMNA):c.357-4696T>C
NM_170707.4(LMNA):c.357-4760T>C
NM_170707.4(LMNA):c.438C>T (p.Ala146=) rs80356805
NM_170707.4(LMNA):c.513+175T>C
NM_170707.4(LMNA):c.513+274C>G
NM_170707.4(LMNA):c.514-111C>T
NM_170707.4(LMNA):c.514-197A>C
NM_170707.4(LMNA):c.51C>T (p.Ser17=) rs11549668
NM_170707.4(LMNA):c.612G>A (p.Leu204=) rs12117552
NM_170707.4(LMNA):c.639+56G>T
NM_170707.4(LMNA):c.639+73C>T
NM_170707.4(LMNA):c.810+61C>T rs11264445
NM_170707.4(LMNA):c.861T>C (p.Ala287=) rs538089
NM_170707.4(LMNA):c.936+234C>T
NM_170707.4(LMNA):c.937-275A>G

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