ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 122
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HGVS dbSNP gnomAD frequency
NM_170707.4(LMNA):c.1930C>T (p.Arg644Cys) rs142000963 0.00117
NM_170707.4(LMNA):c.1912G>A (p.Gly638Arg) rs144851946 0.00063
NM_170707.4(LMNA):c.1634G>A (p.Arg545His) rs142191737 0.00025
NM_170707.4(LMNA):c.1657G>A (p.Asp553Asn) rs373671419 0.00016
NM_170707.4(LMNA):c.1201C>T (p.Arg401Cys) rs61094188 0.00015
NM_170707.4(LMNA):c.1718C>T (p.Ser573Leu) rs60890628 0.00011
NM_170707.4(LMNA):c.1978A>G (p.Asn660Asp) rs374926367 0.00011
NM_170707.4(LMNA):c.1202G>A (p.Arg401His) rs141490569 0.00010
NM_170707.4(LMNA):c.1390A>G (p.Met464Val) rs200262654 0.00009
NM_170707.4(LMNA):c.976T>A (p.Ser326Thr) rs56851164 0.00009
NM_170707.4(LMNA):c.1381-5G>A rs730880133 0.00008
NM_170707.4(LMNA):c.1488+6T>G rs369642101 0.00008
NM_170707.4(LMNA):c.1862C>T (p.Thr621Met) rs765594825 0.00008
NM_170707.4(LMNA):c.1243G>A (p.Val415Ile) rs267607606 0.00007
NM_005572.4(LMNA):c.1714C>T (p.Arg572Cys) rs773169005 0.00006
NM_170707.4(LMNA):c.1567G>A (p.Gly523Arg) rs201583907 0.00006
NM_170707.4(LMNA):c.937-7C>G rs267607681 0.00006
NM_170707.4(LMNA):c.*666_*667del rs941656503 0.00004
NM_170707.4(LMNA):c.1196G>A (p.Arg399His) rs267607563 0.00004
NM_170707.4(LMNA):c.1376A>G (p.Asn459Ser) rs372011095 0.00004
NM_170707.4(LMNA):c.1556C>T (p.Thr519Ile) rs753988867 0.00004
NM_170707.4(LMNA):c.692A>G (p.Asn231Ser) rs760388350 0.00004
NM_170707.4(LMNA):c.848A>G (p.Asn283Ser) rs765241364 0.00004
NM_170707.4(LMNA):c.1001G>A (p.Ser334Asn) rs370656306 0.00003
NM_170707.4(LMNA):c.1324G>A (p.Val442Met) rs368542816 0.00003
NM_170707.4(LMNA):c.1517A>C (p.His506Pro) rs878855233 0.00003
NM_170707.4(LMNA):c.-1C>A rs886043355 0.00002
NM_170707.4(LMNA):c.1190G>A (p.Arg397His) rs747952058 0.00002
NM_170707.4(LMNA):c.1279C>T (p.Arg427Cys) rs373584456 0.00002
NM_170707.4(LMNA):c.1748C>T (p.Ser583Leu) rs59601651 0.00002
NM_170707.4(LMNA):c.1919A>G (p.Asn640Ser) rs752598065 0.00002
NM_170707.4(LMNA):c.290A>C (p.Lys97Thr) rs1060502216 0.00002
NM_170707.4(LMNA):c.295C>A (p.Arg99Ser) rs886045364 0.00002
NM_170707.4(LMNA):c.566G>A (p.Arg189Gln) rs766856162 0.00002
NM_170707.4(LMNA):c.647G>A (p.Arg216His) rs757041809 0.00002
NM_170707.4(LMNA):c.884C>T (p.Ser295Leu) rs769210828 0.00002
NM_170707.4(LMNA):c.977C>T (p.Ser326Leu) rs745540806 0.00002
NM_170707.4(LMNA):c.986G>A (p.Arg329His) rs397517913 0.00002
NM_170707.4(LMNA):c.*672T>C rs879254141 0.00001
NM_170707.4(LMNA):c.*707A>G rs1038556505 0.00001
NM_170707.4(LMNA):c.1016C>A (p.Ala339Glu) rs756538414 0.00001
NM_170707.4(LMNA):c.1027C>T (p.Arg343Trp) rs749784223 0.00001
NM_170707.4(LMNA):c.111G>A (p.Glu37=) rs886038906 0.00001
NM_170707.4(LMNA):c.1184C>T (p.Ser395Leu) rs267607561 0.00001
NM_170707.4(LMNA):c.1195C>T (p.Arg399Cys) rs58672172 0.00001
NM_170707.4(LMNA):c.1280G>A (p.Arg427His) rs747139279 0.00001
NM_170707.4(LMNA):c.1306A>G (p.Thr436Ala) rs876657849 0.00001
NM_170707.4(LMNA):c.1307C>T (p.Thr436Ile) rs773638171 0.00001
NM_170707.4(LMNA):c.1487C>T (p.Thr496Met) rs200466188 0.00001
NM_170707.4(LMNA):c.1600A>T (p.Thr534Ser) rs1311820114 0.00001
NM_170707.4(LMNA):c.1660G>A (p.Glu554Lys) rs71630616 0.00001
NM_170707.4(LMNA):c.1751G>A (p.Arg584His) rs56657623 0.00001
NM_170707.4(LMNA):c.1786G>A (p.Asp596Asn) rs769561386 0.00001
NM_170707.4(LMNA):c.1825G>A (p.Gly609Arg) rs397517898 0.00001
NM_170707.4(LMNA):c.1871G>A (p.Arg624His) rs13768 0.00001
NM_170707.4(LMNA):c.1880G>A (p.Arg627His) rs745997478 0.00001
NM_170707.4(LMNA):c.565C>T (p.Arg189Trp) rs267607626 0.00001
NM_170707.4(LMNA):c.571G>A (p.Val191Met) rs879253896 0.00001
NM_170707.4(LMNA):c.704G>A (p.Arg235His) rs759829161 0.00001
NM_170707.4(LMNA):c.718C>T (p.Arg240Trp) rs775964460 0.00001
NM_170707.4(LMNA):c.749C>T (p.Ala250Val) rs397517907 0.00001
NM_170707.4(LMNA):c.952G>A (p.Ala318Thr) rs267607574 0.00001
NM_005572.4(LMNA):c.1711C>A (p.Arg571Ser) rs80338938
NM_005572.4(LMNA):c.1711_1712delinsTC (p.Arg571Ser) rs794728612
NM_170707.4(LMNA):c.*663G>C
NM_170707.4(LMNA):c.1006C>T (p.Arg336Trp) rs1237093879
NM_170707.4(LMNA):c.1039G>A (p.Glu347Lys) rs267607548
NM_170707.4(LMNA):c.1042A>G (p.Met348Val) rs2102887599
NM_170707.4(LMNA):c.1070A>G (p.Asp357Gly)
NM_170707.4(LMNA):c.1081G>C (p.Glu361Gln) rs267607634
NM_170707.4(LMNA):c.10C>G (p.Pro4Ala)
NM_170707.4(LMNA):c.1106T>C (p.Leu369Pro) rs397517886
NM_170707.4(LMNA):c.1109A>G (p.Asp370Gly)
NM_170707.4(LMNA):c.1123G>A (p.Ala375Thr) rs879254162
NM_170707.4(LMNA):c.1148A>G (p.Glu383Gly) rs1448774273
NM_170707.4(LMNA):c.1158G>C (p.Arg386Ser) rs879253933
NM_170707.4(LMNA):c.1160T>C (p.Leu387Pro) rs879253934
NM_170707.4(LMNA):c.1161_1178dup (p.Arg388_Pro393dup) rs1553265793
NM_170707.4(LMNA):c.1342G>A (p.Glu448Lys) rs2102891243
NM_170707.4(LMNA):c.1453C>G (p.Pro485Ala) rs886042993
NM_170707.4(LMNA):c.1459T>C (p.Phe487Leu) rs1651700215
NM_170707.4(LMNA):c.145G>C (p.Val49Leu) rs879254200
NM_170707.4(LMNA):c.1472C>T (p.Ala491Val) rs2102894241
NM_170707.4(LMNA):c.1504G>C (p.Ala502Pro) rs1215424724
NM_170707.4(LMNA):c.1525C>A (p.Pro509Thr) rs762847359
NM_170707.4(LMNA):c.1529C>T (p.Thr510Ile) rs879254163
NM_170707.4(LMNA):c.1532A>G (p.Asp511Gly) rs2102895367
NM_170707.4(LMNA):c.1552A>G (p.Asn518Asp) rs757733890
NM_170707.4(LMNA):c.1567G>C (p.Gly523Arg) rs201583907
NM_170707.4(LMNA):c.1601C>T (p.Thr534Ile) rs144740174
NM_170707.4(LMNA):c.1609-8C>G rs879253917
NM_170707.4(LMNA):c.161C>T (p.Thr54Met) rs879253992
NM_170707.4(LMNA):c.1639G>A (p.Val547Met) rs201947393
NM_170707.4(LMNA):c.1685T>A (p.Leu562His) rs1057156731
NM_170707.4(LMNA):c.1754C>T (p.Thr585Ile)
NM_170707.4(LMNA):c.1844C>G (p.Ser615Cys) rs879253982
NM_170707.4(LMNA):c.1900G>A (p.Gly634Ser) rs879254188
NM_170707.4(LMNA):c.1948A>C (p.Asn650His) rs2102902603
NM_170707.4(LMNA):c.1949A>G (p.Asn650Ser) rs775728847
NM_170707.4(LMNA):c.1969-1G>T rs1060499873
NM_170707.4(LMNA):c.213C>A (p.Ser71Arg)
NM_170707.4(LMNA):c.242A>G (p.Tyr81Cys) rs879254319
NM_170707.4(LMNA):c.263C>T (p.Ala88Val) rs869025455
NM_170707.4(LMNA):c.272C>T (p.Thr91Ile) rs1306829976
NM_170707.4(LMNA):c.286G>T (p.Ala96Ser) rs1553262000
NM_170707.4(LMNA):c.311T>G (p.Leu104Arg) rs886042953
NM_170707.4(LMNA):c.313_314delinsTT (p.Glu105Leu) rs2102818950
NM_170707.4(LMNA):c.329G>C (p.Arg110Pro) rs556237236
NM_170707.4(LMNA):c.335A>T (p.Glu112Val) rs794728587
NM_170707.4(LMNA):c.356G>C (p.Arg119Pro) rs397517902
NM_170707.4(LMNA):c.357-3734G>A rs888010397
NM_170707.4(LMNA):c.622A>C (p.Lys208Gln) rs770744765
NM_170707.4(LMNA):c.737A>G (p.Gln246Arg) rs794728592
NM_170707.4(LMNA):c.739G>A (p.Glu247Lys) rs727504373
NM_170707.4(LMNA):c.760G>A (p.Asp254Asn) rs1553265346
NM_170707.4(LMNA):c.767T>C (p.Val256Ala)
NM_170707.4(LMNA):c.808A>C (p.Lys270Gln) rs879253920
NM_170707.4(LMNA):c.897C>G (p.Ile299Met) rs762718963
NM_170707.4(LMNA):c.937-8C>G rs751707982
NM_170707.4(LMNA):c.962G>A (p.Arg321Gln) rs1180922815
NM_170707.4(LMNA):c.985C>T (p.Arg329Cys) rs775159300
NM_170707.4(LMNA):c.998C>G (p.Thr333Ser) rs763069566

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