ClinVar Miner

List of variants in gene LAMA4 reported as benign by DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
NM_001105206.3(LAMA4):c.2810A>G (p.Glu937Gly) rs35605307
NM_001105206.3(LAMA4):c.3239G>A (p.Arg1080Gln) rs41289902
NM_001105206.3(LAMA4):c.3283-15C>T rs2032568
NM_001105206.3(LAMA4):c.3349G>A (p.Gly1117Ser) rs2032567
NM_001105206.3(LAMA4):c.3356C>G (p.Pro1119Arg) rs1050349
NM_001105206.3(LAMA4):c.4646A>G (p.Asn1549Ser) rs12110554
NM_001105206.3(LAMA4):c.4716C>T (p.Leu1572=) rs35679345
NM_001105206.3(LAMA4):c.5160T>A (p.Val1720=) rs1050353
NM_001105206.3(LAMA4):c.5326+15A>C rs3734290
NM_001105206.3(LAMA4):c.5326+6T>G rs3734289
NM_001105206.3(LAMA4):c.5443G>A (p.Val1815Ile) rs3734292

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.