List of variants in gene LMNA reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 64

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.*639G>A	rs185169879	0.00928
NM_170707.4(LMNA):c.1699-133C>T	rs35917802	0.00391
NM_005572.3(LMNA):c.-223C>T	rs188625872	0.00284
NM_170707.4(LMNA):c.*130T>G	rs181732923	0.00211
NM_170707.4(LMNA):c.640-52C>T	rs41314033	0.00091
NM_170707.4(LMNA):c.1804G>A (p.Gly602Ser)	rs60662302	0.00078
NM_170707.4(LMNA):c.1584G>A (p.Thr528=)	rs80356812	0.00029
NM_170707.4(LMNA):c.192C>T (p.Thr64=)	rs137969290	0.00028
NM_170707.4(LMNA):c.1017G>A (p.Ala339=)	rs17847242	0.00021
NM_170707.4(LMNA):c.895A>G (p.Ile299Val)	rs150924946	0.00016
NM_170707.4(LMNA):c.1051A>C (p.Arg351=)	rs771623461	0.00013
NM_170707.4(LMNA):c.1488+14C>T	rs377700689	0.00013
NM_170707.4(LMNA):c.811-12C>T	rs372962650	0.00012
NM_170707.4(LMNA):c.990G>A (p.Glu330=)	rs140800215	0.00012
NM_170707.4(LMNA):c.1314G>A (p.Gly438=)	rs774817302	0.00011
NM_170707.4(LMNA):c.150C>T (p.Arg50=)	rs397517894	0.00009
NM_170707.4(LMNA):c.1381-6C>T	rs371635492	0.00006
NM_170707.4(LMNA):c.1770C>T (p.Thr590=)	rs397517896	0.00006
NM_170707.4(LMNA):c.1311C>T (p.Ser437=)	rs763224059	0.00004
NM_170707.4(LMNA):c.1698+25C>T	rs727504435	0.00004
NM_170707.4(LMNA):c.726G>A (p.Ala242=)	rs763625309	0.00004
NM_170707.4(LMNA):c.936+12C>T	rs199881992	0.00004
NM_170707.4(LMNA):c.1380+18G>A	rs777846700	0.00003
NM_170707.4(LMNA):c.1489-9C>T	rs374324602	0.00003
NM_170707.4(LMNA):c.937-8C>A	rs751707982	0.00003
NM_170707.4(LMNA):c.1071C>T (p.Asp357=)	rs376875762	0.00002
NM_170707.4(LMNA):c.1157+18C>T	rs372021174	0.00002
NM_170707.4(LMNA):c.1755C>T (p.Thr585=)	rs545752475	0.00002
NM_170707.4(LMNA):c.1857T>C (p.Ser619=)	rs368581237	0.00002
NM_170707.4(LMNA):c.294G>A (p.Glu98=)	rs886045363	0.00002
NM_170707.4(LMNA):c.-28C>T	rs1404811179	0.00001
NM_170707.4(LMNA):c.-42C>T	rs761922735	0.00001
NM_170707.4(LMNA):c.1157+19G>A	rs757715731	0.00001
NM_170707.4(LMNA):c.1488+15G>A	rs371380638	0.00001
NM_170707.4(LMNA):c.1488+8G>A	rs762836610	0.00001
NM_170707.4(LMNA):c.153G>T (p.Ser51=)	rs751886390	0.00001
NM_170707.4(LMNA):c.1605G>A (p.Gly535=)	rs769398087	0.00001
NM_170707.4(LMNA):c.1662G>A (p.Glu554=)	rs201936898	0.00001
NM_170707.4(LMNA):c.1680C>T (p.Asp560=)	rs17847249	0.00001
NM_170707.4(LMNA):c.1699-8C>G	rs727503137	0.00001
NM_170707.4(LMNA):c.1764C>T (p.Cys588=)	rs759016336	0.00001
NM_170707.4(LMNA):c.1773C>T (p.Cys591=)	rs397517897	0.00001
NM_170707.4(LMNA):c.1863G>A (p.Thr621=)	rs749999967	0.00001
NM_170707.4(LMNA):c.240C>T (p.Ala80=)	rs780194620	0.00001
NM_170707.4(LMNA):c.356+18G>T	rs764535819	0.00001
NM_170707.4(LMNA):c.514-11C>T	rs886045365	0.00001
NM_170707.4(LMNA):c.639+12G>A	rs1451785437	0.00001
NM_170707.4(LMNA):c.936+19C>T	rs201664413	0.00001
NM_170707.4(LMNA):c.948G>A (p.Lys316=)	rs778421025	0.00001
NM_170707.4(LMNA):c.954G>A (p.Ala318=)	rs397517914	0.00001
NM_170707.4(LMNA):c.*484AG[9]	rs748490381
NM_170707.4(LMNA):c.*749G>A	rs1057521412
NM_170707.4(LMNA):c.1029G>C (p.Arg343=)	rs1553265680
NM_170707.4(LMNA):c.1209C>T (p.Ser403=)	rs776975256
NM_170707.4(LMNA):c.1317C>T (p.Arg439=)	rs374804871
NM_170707.4(LMNA):c.1380+5dup	rs2102891660
NM_170707.4(LMNA):c.1413C>G (p.Arg471=)	rs1572365626
NM_170707.4(LMNA):c.1609-9C>T	rs1057522558
NM_170707.4(LMNA):c.1698+25C>G	rs727504435
NM_170707.4(LMNA):c.1968+12C>G	rs1458573927
NM_170707.4(LMNA):c.526C>T (p.Leu176=)	rs149113760
NM_170707.4(LMNA):c.657G>A (p.Lys219=)	rs1553265267
NM_170707.4(LMNA):c.811-18del	rs1553265425
NM_170707.4(LMNA):c.927C>A (p.Leu309=)	rs752558753

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