ClinVar Miner

List of variants in gene LAMA4 reported as uncertain significance for Primary dilated cardiomyopathy

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NM_001105206.3(LAMA4):c.1121G>A (p.Ser374Asn) rs869025449
NM_001105206.3(LAMA4):c.1999G>T (p.Asp667Tyr) rs397516720
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519
NM_001105206.3(LAMA4):c.2493G>A (p.Lys831=) rs869025450
NM_001105206.3(LAMA4):c.3742A>G (p.Ile1248Val) rs547323858
NM_001105206.3(LAMA4):c.631A>C (p.Asn211His) rs371848733

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.