List of variants in gene LMNA reported as uncertain significance for Dilated cardiomyopathy 1A

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: 47

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.811-13T>A	rs80356809	0.00309
NM_005572.3(LMNA):c.-223C>T	rs188625872	0.00284
NM_170707.4(LMNA):c.1566C>T (p.Cys522=)	rs149339264	0.00123
NM_170707.4(LMNA):c.1930C>T (p.Arg644Cys)	rs142000963	0.00117
NM_170707.4(LMNA):c.1634G>A (p.Arg545His)	rs142191737	0.00025
NM_170707.4(LMNA):c.1698+83G>A	rs555844506	0.00023
NM_170707.4(LMNA):c.1488+14C>T	rs377700689	0.00013
NM_170707.4(LMNA):c.-138T>C	rs886045359	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.1567G>A (p.Gly523Arg)	rs201583907	0.00006
NM_170707.4(LMNA):c.350A>G (p.Lys117Arg)	rs397517901	0.00004
NM_170707.4(LMNA):c.692A>G (p.Asn231Ser)	rs760388350	0.00004
NM_170707.4(LMNA):c.1227A>G (p.Thr409=)	rs762130433	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.1699-7T>C	rs771074100	0.00003
NM_170707.4(LMNA):c.937-8C>A	rs751707982	0.00003
NM_170707.4(LMNA):c.-44T>A	rs1185731069	0.00002
NM_170707.4(LMNA):c.1698+57G>A	rs557334569	0.00002
NM_170707.4(LMNA):c.294G>A (p.Glu98=)	rs886045363	0.00002
NM_170707.4(LMNA):c.295C>A (p.Arg99Ser)	rs886045364	0.00002
NM_005572.3(LMNA):c.-210T>C	rs886045356	0.00001
NM_170707.4(LMNA):c.1027C>T (p.Arg343Trp)	rs749784223	0.00001
NM_170707.4(LMNA):c.1358G>A (p.Arg453Gln)	rs267607598	0.00001
NM_170707.4(LMNA):c.1487C>T (p.Thr496Met)	rs200466188	0.00001
NM_170707.4(LMNA):c.1871G>A (p.Arg624His)	rs13768	0.00001
NM_170707.4(LMNA):c.514-11C>T	rs886045365	0.00001
NM_170707.4(LMNA):c.749C>T (p.Ala250Val)	rs397517907	0.00001
NM_170707.4(LMNA):c.953C>T (p.Ala318Val)	rs1212920276	0.00001
NM_170707.4(LMNA):c.985C>G (p.Arg329Gly)	rs775159300	0.00001
NM_005572.3(LMNA):c.-226C>T	rs886045354
NM_170707.4(LMNA):c.1070A>T (p.Asp357Val)	rs1131690785
NM_170707.4(LMNA):c.1123G>A (p.Ala375Thr)	rs879254162
NM_170707.4(LMNA):c.1338T>G (p.Asp446Glu)	rs505058
NM_170707.4(LMNA):c.133T>C (p.Tyr45His)	rs1649714371
NM_170707.4(LMNA):c.1445G>T (p.Arg482Leu)	rs11575937
NM_170707.4(LMNA):c.1488G>C (p.Thr496=)	rs375516745
NM_170707.4(LMNA):c.1678G>A (p.Asp560Asn)	rs1651791067
NM_170707.4(LMNA):c.193G>C (p.Glu65Gln)	rs1168314722
NM_170707.4(LMNA):c.356+12C>A	rs1649747809
NM_170707.4(LMNA):c.796A>G (p.Thr266Ala)	rs1651418246
NM_170707.4(LMNA):c.810+17G>A	rs771192755
NM_170707.4(LMNA):c.890T>A (p.Ile297Asn)	rs1060502212
NM_170707.4(LMNA):c.937-5T>C	rs1001248677
NM_170707.4(LMNA):c.969GGA[1] (p.Glu324del)
NM_170707.4(LMNA):c.985C>A (p.Arg329Ser)	rs775159300

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