ClinVar Miner

List of variants in gene LMNA reported as uncertain significance for Cardiomyopathy

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Total variants: 19
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HGVS dbSNP
NM_170707.4(LMNA):c.1004G>A (p.Arg335Gln) rs138592977
NM_170707.4(LMNA):c.1201C>T (p.Arg401Cys) rs61094188
NM_170707.4(LMNA):c.1232G>A (p.Gly411Asp) rs267607647
NM_170707.4(LMNA):c.1262T>C (p.Leu421Pro) rs267607564
NM_170707.4(LMNA):c.1327G>A (p.Glu443Lys) rs1558132212
NM_170707.4(LMNA):c.1381-6C>A rs371635492
NM_170707.4(LMNA):c.1390A>G (p.Met464Val) rs200262654
NM_170707.4(LMNA):c.1517A>C (p.His506Pro) rs878855233
NM_170707.4(LMNA):c.1634G>A (p.Arg545His) rs142191737
NM_170707.4(LMNA):c.1699-8C>G rs727503137
NM_170707.4(LMNA):c.1749G>A (p.Ser583=) rs970494454
NM_170707.4(LMNA):c.178C>T (p.Arg60Cys) rs28928900
NM_170707.4(LMNA):c.1880G>A (p.Arg627His) rs745997478
NM_170707.4(LMNA):c.1931G>A (p.Arg644His) rs368386019
NM_170707.4(LMNA):c.386C>A (p.Ala129Asp) rs768203943
NM_170707.4(LMNA):c.497G>A (p.Arg166Gln) rs267607570
NM_170707.4(LMNA):c.647G>A (p.Arg216His) rs757041809
NM_170707.4(LMNA):c.884C>T (p.Ser295Leu) rs769210828
NM_170707.4(LMNA):c.937-7C>G rs267607681

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