List of variants in gene LAMA2 studied for Primary 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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000426.4(LAMA2):c.8905C>T (p.Arg2969Cys)	rs374888837	0.00021
NM_000426.4(LAMA2):c.7057C>T (p.Arg2353Cys)	rs145885540	0.00016
NM_000426.4(LAMA2):c.8842G>A (p.Gly2948Ser)	rs143638361	0.00011
NM_000426.4(LAMA2):c.2735C>T (p.Ala912Val)	rs376580266	0.00003
NM_000426.4(LAMA2):c.470C>G (p.Ser157Cys)	rs756699354	0.00001
NM_000426.4(LAMA2):c.4607C>T (p.Pro1536Leu)	rs1776956586
NM_000426.4(LAMA2):c.7040G>T (p.Gly2347Val)	rs529981007
NM_000426.4(LAMA2):c.7525_7528dup (p.Ser2510fs)	rs2114834553

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.