ClinVar Miner

List of variants in gene LAMP2 reported as likely pathogenic for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
NM_002294.2(LAMP2):c.1075C>T (p.Gln359Ter) rs1057517940
NM_002294.2(LAMP2):c.183+5G>A rs730880479
NM_002294.2(LAMP2):c.184-1G>T rs1064796635
NM_002294.2(LAMP2):c.1A>T (p.Met1Leu) rs1556124149
NM_002294.2(LAMP2):c.929-1G>A rs727504262
NM_013995.2(LAMP2):c.659dup (p.Gly221fs) rs1556101640
NM_013995.2(LAMP2):c.669T>G (p.Tyr223Ter)
NM_013995.2(LAMP2):c.834del (p.Ile279fs)

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.