ClinVar Miner

List of variants in gene LMNA, LOC126805877 studied for Cardiomyopathy

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_170707.4(LMNA):c.438C>T (p.Ala146=) rs80356805 0.00738
NM_170707.4(LMNA):c.357C>T (p.Arg119=) rs41313880 0.00321
NM_170707.4(LMNA):c.471G>A (p.Thr157=) rs150645079 0.00008
NM_170707.4(LMNA):c.497G>A (p.Arg166Gln) rs267607570 0.00005
NM_170707.4(LMNA):c.357-8T>C rs1053291240 0.00004
NM_170707.4(LMNA):c.467G>A (p.Arg156His) rs764475194 0.00004
NM_170707.4(LMNA):c.364A>G (p.Lys122Glu) rs1222398892 0.00002
NM_170707.4(LMNA):c.357-13C>A rs1264489096 0.00001
NM_170707.4(LMNA):c.357-15C>T rs779619961 0.00001
NM_170707.4(LMNA):c.369G>A (p.Lys123=) rs367938270 0.00001
NM_170707.4(LMNA):c.398G>A (p.Arg133Gln) rs60864230 0.00001
NM_170707.4(LMNA):c.451G>A (p.Ala151Thr) rs766291714 0.00001
NM_170707.4(LMNA):c.478G>C (p.Gly160Arg) rs765665953 0.00001
NM_170707.4(LMNA):c.480C>A (p.Gly160=) rs758848135 0.00001
NM_170707.4(LMNA):c.480C>T (p.Gly160=) rs758848135 0.00001
NM_170707.4(LMNA):c.496C>T (p.Arg166Trp) rs370200334 0.00001
NM_170707.4(LMNA):c.370G>A (p.Glu124Lys) rs2102865393
NM_170707.4(LMNA):c.373G>A (p.Gly125Ser) rs267607605
NM_170707.4(LMNA):c.375T>C (p.Gly125=) rs1164862537
NM_170707.4(LMNA):c.379C>T (p.Leu127=) rs1428192739
NM_170707.4(LMNA):c.382A>G (p.Ile128Val) rs1338283666
NM_170707.4(LMNA):c.383T>C (p.Ile128Thr) rs746475627
NM_170707.4(LMNA):c.386C>A (p.Ala129Asp) rs768203943
NM_170707.4(LMNA):c.449C>T (p.Thr150Ile) rs869069617
NM_170707.4(LMNA):c.470C>A (p.Thr157Lys) rs754097769
NM_170707.4(LMNA):c.481G>A (p.Glu161Lys) rs28933093
NM_170707.4(LMNA):c.486G>A (p.Leu162=) rs727503135
NM_170707.4(LMNA):c.488A>G (p.His163Arg) rs1650987918
NM_170707.4(LMNA):c.489T>G (p.His163Gln) rs1558126350
NM_170707.4(LMNA):c.503A>G (p.Gln168Arg) rs1371187616
NM_170707.4(LMNA):c.511A>G (p.Lys171Glu) rs1650991296
NM_170707.4(LMNA):c.513+8del rs1650992817

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