ClinVar Miner

List of variants in gene LAMA2 reported as pathogenic by Counsyl

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
NM_000426.3(LAMA2):c.1122del (p.Gly376fs) rs1338860420
NM_000426.3(LAMA2):c.1303C>T (p.Arg435Ter) rs773209126
NM_000426.3(LAMA2):c.2230C>T (p.Arg744Ter) rs775676341
NM_000426.3(LAMA2):c.3085C>T (p.Arg1029Ter) rs145420388
NM_000426.3(LAMA2):c.363C>A (p.Tyr121Ter) rs535635043
NM_000426.3(LAMA2):c.3799_3821del (p.Phe1267fs) rs750220830
NM_000426.3(LAMA2):c.3976C>T (p.Arg1326Ter) rs398123373
NM_000426.3(LAMA2):c.4048C>T (p.Arg1350Ter) rs756854513
NM_000426.3(LAMA2):c.4645C>T (p.Arg1549Ter) rs121913575
NM_000426.3(LAMA2):c.5116C>T (p.Arg1706Ter) rs758775001
NM_000426.3(LAMA2):c.5156_5159del (p.Lys1719fs) rs1554286963
NM_000426.3(LAMA2):c.5476C>T (p.Arg1826Ter) rs747349942
NM_000426.3(LAMA2):c.7147C>T (p.Arg2383Ter) rs121913576
NM_000426.3(LAMA2):c.7490_7493dup (p.Asp2498fs) rs1480934961
NM_000426.3(LAMA2):c.7732C>T (p.Arg2578Ter) rs121913572
NM_000426.3(LAMA2):c.8244+1G>A rs749522728

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.