List of variants in gene LAMP2 reported by Mayo Clinic Laboratories, Mayo Clinic

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002294.3(LAMP2):c.156A>T (p.Val52=)	rs12097	0.39300
NM_002294.3(LAMP2):c.927C>T (p.Ser309=)	rs73219144	0.02702
NM_002294.3(LAMP2):c.1093+2514G>A	rs144140265	0.00396
NM_002294.3(LAMP2):c.1093+2544A>G	rs777128122	0.00009
NM_002294.3(LAMP2):c.32G>T (p.Gly11Val)	rs3180515	0.00005
NM_002294.3(LAMP2):c.472A>G (p.Thr158Ala)	rs138374063	0.00003
NM_002294.3(LAMP2):c.415G>A (p.Glu139Lys)	rs373007615	0.00002
NM_002294.3(LAMP2):c.-23_-16del	rs1556124290
NM_002294.3(LAMP2):c.-32GTCGCCGCC[1]	rs193922648
NM_002294.3(LAMP2):c.581C>A (p.Thr194Asn)	rs1033442580

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.