List of variants in gene LMNA studied for Primary familial dilated cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.1201C>T (p.Arg401Cys)	rs61094188	0.00015
NM_170707.4(LMNA):c.992G>A (p.Arg331Gln)	rs59301204	0.00004
NM_170707.4(LMNA):c.*722T>C	rs921268252	0.00001
NM_170707.4(LMNA):c.1003C>T (p.Arg335Trp)	rs386134243	0.00001
NM_170707.4(LMNA):c.274C>T (p.Leu92Phe)	rs267607560	0.00001
NM_170707.4(LMNA):c.646C>T (p.Arg216Cys)	rs794728591	0.00001
NM_170707.4(LMNA):c.725C>T (p.Ala242Val)	rs397517906	0.00001
NM_170707.4(LMNA):c.949G>A (p.Glu317Lys)	rs56816490	0.00001
NM_170707.4(LMNA):c.1494G>A (p.Trp498Ter)	rs57730570
NM_170707.4(LMNA):c.1494G>T (p.Trp498Cys)	rs57730570
NM_170707.4(LMNA):c.296G>C (p.Arg99Pro)	rs1572332762
NM_170707.4(LMNA):c.334G>A (p.Glu112Lys)	rs1553262031
NM_170707.4(LMNA):c.611T>A (p.Leu204Gln)	rs1553265180
NM_170707.4(LMNA):c.961C>T (p.Arg321Ter)	rs267607554

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.