ClinVar Miner

List of variants in gene LMNA reported as uncertain significance by GeneDx

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Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP
NM_001257374.2(LMNA):c.665G>A (p.Ser222Asn) rs370656306
NM_005572.3(LMNA):c.111G>A (p.Glu37=) rs886038906
NM_005572.3(LMNA):c.1201C>T (p.Arg401Cys) rs61094188
NM_005572.3(LMNA):c.1376A>G (p.Asn459Ser) rs372011095
NM_005572.3(LMNA):c.1711_1712delCGinsTC (p.Arg571Ser) rs794728612
NM_005572.3(LMNA):c.295C>A (p.Arg99Ser) rs886045364
NM_170707.2(LMNA):c.-1C>A rs886043355
NM_170707.2(LMNA):c.1081G>C (p.Glu361Gln) rs267607634
NM_170707.2(LMNA):c.1123G>A (p.Ala375Thr) rs879254162
NM_170707.2(LMNA):c.1158G>C (p.Arg386Ser) rs879253933
NM_170707.2(LMNA):c.1280G>A (p.Arg427His) rs747139279
NM_170707.2(LMNA):c.1390A>G (p.Met464Val) rs200262654
NM_170707.2(LMNA):c.145G>C (p.Val49Leu) rs879254200
NM_170707.2(LMNA):c.1488+6T>G rs369642101
NM_170707.2(LMNA):c.1529C>T (p.Thr510Ile) rs879254163
NM_170707.2(LMNA):c.1567G>C (p.Gly523Arg) rs201583907
NM_170707.2(LMNA):c.1600A>T (p.Thr534Ser) rs1311820114
NM_170707.2(LMNA):c.1601C>T (p.Thr534Ile) rs144740174
NM_170707.2(LMNA):c.1609-8C>G rs879253917
NM_170707.2(LMNA):c.1685T>A (p.Leu562His) rs1057156731
NM_170707.2(LMNA):c.1698+16C>T rs773169005
NM_170707.2(LMNA):c.1751G>A (p.Arg584His) rs56657623
NM_170707.2(LMNA):c.1844C>G (p.Ser615Cys) rs879253982
NM_170707.2(LMNA):c.1900G>A (p.Gly634Ser) rs879254188
NM_170707.2(LMNA):c.242A>G (p.Tyr81Cys) rs879254319
NM_170707.2(LMNA):c.263C>T (p.Ala88Val) rs869025455
NM_170707.2(LMNA):c.311T>G (p.Leu104Arg) rs886042953
NM_170707.2(LMNA):c.335A>T (p.Glu112Val) rs794728587
NM_170707.2(LMNA):c.356G>C (p.Arg119Pro) rs397517902
NM_170707.2(LMNA):c.357-4406A>G rs879254318
NM_170707.2(LMNA):c.408C>A (p.Asp136Glu) rs879253923
NM_170707.2(LMNA):c.470C>G (p.Thr157Arg) rs754097769
NM_170707.2(LMNA):c.504G>C (p.Gln168His) rs747771347
NM_170707.2(LMNA):c.566G>A (p.Arg189Gln) rs766856162
NM_170707.2(LMNA):c.656A>C (p.Lys219Thr) rs267607584
NM_170707.2(LMNA):c.737A>G (p.Gln246Arg) rs794728592
NM_170707.2(LMNA):c.760G>A (p.Asp254Asn) rs1553265346
NM_170707.2(LMNA):c.77T>C (p.Ile26Thr) rs794728600
NM_170707.2(LMNA):c.808A>C (p.Lys270Gln) rs879253920
NM_170707.2(LMNA):c.991C>T (p.Arg331Trp) rs879253898
NM_170707.2(LMNA):c.998C>G (p.Thr333Ser) rs763069566
NM_170707.3(LMNA):c.*672T>C rs879254141
NM_170707.3(LMNA):c.*707A>G rs1038556505
NM_170707.3(LMNA):c.1004G>A (p.Arg335Gln) rs138592977
NM_170707.3(LMNA):c.1106T>C (p.Leu369Pro) rs397517886
NM_170707.3(LMNA):c.1160T>C (p.Leu387Pro) rs879253934
NM_170707.3(LMNA):c.1190G>A (p.Arg397His) rs747952058
NM_170707.3(LMNA):c.1195C>T (p.Arg399Cys) rs58672172
NM_170707.3(LMNA):c.1196G>A (p.Arg399His) rs267607563
NM_170707.3(LMNA):c.1202G>A (p.Arg401His) rs141490569
NM_170707.3(LMNA):c.1243G>A (p.Val415Ile) rs267607606
NM_170707.3(LMNA):c.1279C>T (p.Arg427Cys) rs373584456
NM_170707.3(LMNA):c.1381-5G>A rs730880133
NM_170707.3(LMNA):c.1487C>T (p.Thr496Met) rs200466188
NM_170707.3(LMNA):c.1517A>C (p.His506Pro) rs878855233
NM_170707.3(LMNA):c.1567G>A (p.Gly523Arg) rs201583907
NM_170707.3(LMNA):c.161C>T (p.Thr54Met) rs879253992
NM_170707.3(LMNA):c.1748C>T (p.Ser583Leu) rs59601651
NM_170707.3(LMNA):c.1912G>A (p.Gly638Arg) rs144851946
NM_170707.3(LMNA):c.1930C>T (p.Arg644Cys) rs142000963
NM_170707.3(LMNA):c.1978A>G (p.Asn660Asp) rs374926367
NM_170707.3(LMNA):c.410T>C (p.Leu137Pro) rs879254302
NM_170707.3(LMNA):c.497G>A (p.Arg166Gln) rs267607570
NM_170707.3(LMNA):c.571G>A (p.Val191Met) rs879253896
NM_170707.3(LMNA):c.647G>A (p.Arg216His) rs757041809
NM_170707.3(LMNA):c.704G>A (p.Arg235His) rs759829161
NM_170707.3(LMNA):c.718C>T (p.Arg240Trp) rs775964460
NM_170707.3(LMNA):c.749C>T (p.Ala250Val) rs397517907
NM_170707.3(LMNA):c.74G>T (p.Arg25Leu) rs61578124
NM_170707.3(LMNA):c.976T>A (p.Ser326Thr) rs56851164
NM_170707.3(LMNA):c.985C>T (p.Arg329Cys) rs775159300
NM_170707.4(LMNA):c.1880G>A (p.Arg627His) rs745997478

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