ClinVar Miner

List of variants in gene LMNA reported as uncertain significance for Cardiovascular phenotype

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Total variants: 25
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HGVS dbSNP
NM_170707.4(LMNA):c.109G>A (p.Glu37Lys) rs1354642495
NM_170707.4(LMNA):c.1324G>A (p.Val442Met) rs368542816
NM_170707.4(LMNA):c.1426G>T (p.Asp476Tyr) rs886039032
NM_170707.4(LMNA):c.149G>A (p.Arg50His) rs60695352
NM_170707.4(LMNA):c.1567G>A (p.Gly523Arg) rs201583907
NM_170707.4(LMNA):c.1634G>A (p.Arg545His) rs142191737
NM_170707.4(LMNA):c.1637C>T (p.Ser546Leu) rs886038995
NM_170707.4(LMNA):c.1698+13_1698+14delinsTC rs794728612
NM_170707.4(LMNA):c.1718C>T (p.Ser573Leu) rs60890628
NM_170707.4(LMNA):c.1748C>T (p.Ser583Leu) rs59601651
NM_170707.4(LMNA):c.1873_1874delinsCC (p.Ser625Pro) rs1553266553
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.236C>A (p.Ala79Asp) rs1553261972
NM_170707.4(LMNA):c.250G>A (p.Glu84Lys) rs794728602
NM_170707.4(LMNA):c.480C>T (p.Gly160=) rs758848135
NM_170707.4(LMNA):c.569G>A (p.Arg190Gln) rs267607571
NM_170707.4(LMNA):c.610C>G (p.Leu204Val) rs1553265177
NM_170707.4(LMNA):c.646C>T (p.Arg216Cys) rs794728591
NM_170707.4(LMNA):c.658C>T (p.Arg220Cys) rs370134870
NM_170707.4(LMNA):c.787C>A (p.Leu263Met) rs750246389
NM_170707.4(LMNA):c.845G>A (p.Ser282Asn) rs1553265438
NM_170707.4(LMNA):c.848A>G (p.Asn283Ser) rs765241364
NM_170707.4(LMNA):c.884C>T (p.Ser295Leu) rs769210828
NM_170707.4(LMNA):c.976T>A (p.Ser326Thr) rs56851164

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