ClinVar Miner

List of variants in gene LMNA reported as likely benign for Cardiomyopathy

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Total variants: 20
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HGVS dbSNP
NM_170707.4(LMNA):c.1155G>A (p.Glu385=) rs878855232
NM_170707.4(LMNA):c.1185G>A (p.Ser395=) rs397517890
NM_170707.4(LMNA):c.12G>A (p.Pro4=) rs369823958
NM_170707.4(LMNA):c.1488G>A (p.Thr496=) rs375516745
NM_170707.4(LMNA):c.1551G>A (p.Gln517=) rs41314035
NM_170707.4(LMNA):c.1659C>T (p.Asp553=) rs748768783
NM_170707.4(LMNA):c.1785C>T (p.Ala595=) rs748139390
NM_170707.4(LMNA):c.1804G>A (p.Gly602Ser) rs60662302
NM_170707.4(LMNA):c.1930C>T (p.Arg644Cys) rs142000963
NM_170707.4(LMNA):c.1931G>A (p.Arg644His) rs368386019
NM_170707.4(LMNA):c.249C>T (p.Ala83=) rs746916710
NM_170707.4(LMNA):c.346C>T (p.Leu116=) rs876657491
NM_170707.4(LMNA):c.357-20C>T rs193922724
NM_170707.4(LMNA):c.471G>A (p.Thr157=) rs150645079
NM_170707.4(LMNA):c.732G>A (p.Ala244=) rs756952925
NM_170707.4(LMNA):c.811-13T>A rs80356809
NM_170707.4(LMNA):c.895A>G (p.Ile299Val) rs150924946
NM_170707.4(LMNA):c.937-8C>A rs751707982
NM_170707.4(LMNA):c.937-8C>G rs751707982
NM_170707.4(LMNA):c.969G>A (p.Leu323=) rs1558130869

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