ClinVar Miner

List of variants in gene LMNA reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP
NM_005572.3(LMNA):c.1017G>A (p.Ala339=) rs17847242
NM_005572.3(LMNA):c.1242C>T (p.Ser414=) rs184946451
NM_005572.3(LMNA):c.1338T>C (p.Asp446=) rs505058
NM_005572.3(LMNA):c.1376A>G (p.Asn459Ser) rs372011095
NM_005572.3(LMNA):c.1584G>A (p.Thr528=) rs80356812
NM_005572.3(LMNA):c.1698C>T (p.His566=) rs4641
NM_005572.3(LMNA):c.198T>C (p.Ser66=) rs397517899
NM_005572.3(LMNA):c.261T>C (p.Asp87=) rs397517900
NM_005572.3(LMNA):c.294G>A (p.Glu98=) rs886045363
NM_005572.3(LMNA):c.357-20C>T rs193922724
NM_005572.3(LMNA):c.438C>T (p.Ala146=) rs80356805
NM_005572.3(LMNA):c.486G>A (p.Leu162=) rs727503135
NM_005572.3(LMNA):c.810+13G>A rs11264444
NM_005572.3(LMNA):c.837G>A (p.Glu279=) rs727505198
NM_005572.3(LMNA):c.861T>C (p.Ala287=) rs538089
NM_005572.3(LMNA):c.927C>A (p.Leu309=) rs752558753
NM_005572.3(LMNA):c.936+12C>T rs199881992
NM_005572.3(LMNA):c.954G>A (p.Ala318=) rs397517914
NM_170707.2(LMNA):c.1185G>A (p.Ser395=) rs397517890
NM_170707.2(LMNA):c.346C>T (p.Leu116=) rs876657491
NM_170707.3(LMNA):c.*749G>A rs1057521412
NM_170707.3(LMNA):c.-28C>T rs1404811179
NM_170707.3(LMNA):c.-42C>T rs761922735
NM_170707.3(LMNA):c.1029G>C (p.Arg343=) rs1553265680
NM_170707.3(LMNA):c.1051A>C (p.Arg351=) rs771623461
NM_170707.3(LMNA):c.1071C>T (p.Asp357=) rs376875762
NM_170707.3(LMNA):c.1122C>T (p.His374=) rs143715750
NM_170707.3(LMNA):c.1157+16G>A rs534807
NM_170707.3(LMNA):c.1157+18C>T rs372021174
NM_170707.3(LMNA):c.1157+19G>A rs757715731
NM_170707.3(LMNA):c.1158-43A>G rs16837198
NM_170707.3(LMNA):c.1209C>T (p.Ser403=) rs776975256
NM_170707.3(LMNA):c.1311C>T (p.Ser437=) rs763224059
NM_170707.3(LMNA):c.1314G>A (p.Gly438=) rs774817302
NM_170707.3(LMNA):c.1317C>T (p.Arg439=) rs374804871
NM_170707.3(LMNA):c.1380+37C>T rs201233721
NM_170707.3(LMNA):c.1381-6C>T rs371635492
NM_170707.3(LMNA):c.1488+14C>T rs377700689
NM_170707.3(LMNA):c.1488+15G>A rs371380638
NM_170707.3(LMNA):c.1488+33G>T rs886038742
NM_170707.3(LMNA):c.1488+8G>A rs762836610
NM_170707.3(LMNA):c.150C>T (p.Arg50=) rs397517894
NM_170707.3(LMNA):c.153G>T (p.Ser51=) rs751886390
NM_170707.3(LMNA):c.1551G>A (p.Gln517=) rs41314035
NM_170707.3(LMNA):c.1566C>T (p.Cys522=) rs149339264
NM_170707.3(LMNA):c.1605G>A (p.Gly535=) rs769398087
NM_170707.3(LMNA):c.1609-9C>T rs1057522558
NM_170707.3(LMNA):c.1656C>T (p.Asp552=) rs370219874
NM_170707.3(LMNA):c.1662G>A (p.Glu554=) rs201936898
NM_170707.3(LMNA):c.1680C>T (p.Asp560=) rs17847249
NM_170707.3(LMNA):c.1698+25C>T rs727504435
NM_170707.3(LMNA):c.1731T>C (p.Ala577=) rs776066211
NM_170707.3(LMNA):c.1761G>A (p.Leu587=) rs80356813
NM_170707.3(LMNA):c.1770C>G (p.Thr590=) rs397517896
NM_170707.3(LMNA):c.1770C>T (p.Thr590=) rs397517896
NM_170707.3(LMNA):c.1773C>T (p.Cys591=) rs397517897
NM_170707.3(LMNA):c.1804G>A (p.Gly602Ser) rs60662302
NM_170707.3(LMNA):c.1857T>C (p.Ser619=) rs368581237
NM_170707.3(LMNA):c.1863G>A (p.Thr621=) rs749999967
NM_170707.3(LMNA):c.1911C>T (p.Phe637=) rs117939448
NM_170707.3(LMNA):c.1912G>A (p.Gly638Arg) rs144851946
NM_170707.3(LMNA):c.192C>T (p.Thr64=) rs137969290
NM_170707.3(LMNA):c.1930C>T (p.Arg644Cys) rs142000963
NM_170707.3(LMNA):c.1968+12C>G rs1458573927
NM_170707.3(LMNA):c.356+18G>T rs764535819
NM_170707.3(LMNA):c.357C>T (p.Arg119=) rs41313880
NM_170707.3(LMNA):c.471G>A (p.Thr157=) rs150645079
NM_170707.3(LMNA):c.526C>T (p.Leu176=) rs149113760
NM_170707.3(LMNA):c.639+12G>A rs1451785437
NM_170707.3(LMNA):c.657G>A (p.Lys219=) rs1553265267
NM_170707.3(LMNA):c.789G>A (p.Leu263=) rs148557956
NM_170707.3(LMNA):c.78C>T (p.Ile26=) rs373721390
NM_170707.3(LMNA):c.811-12C>T rs372962650
NM_170707.3(LMNA):c.811-13T>A rs80356809
NM_170707.3(LMNA):c.811-18delC rs1553265425
NM_170707.3(LMNA):c.895A>G (p.Ile299Val) rs150924946
NM_170707.3(LMNA):c.936+47C>T rs370242860
NM_170707.3(LMNA):c.937-7C>G rs267607681
NM_170707.3(LMNA):c.937-8C>A rs751707982
NM_170707.3(LMNA):c.948G>A (p.Lys316=) rs778421025

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