List of variants in gene LAMP2 reported as benign by Invitae

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_002294.3(LAMP2):c.156A>T (p.Val52=)	rs12097	0.39324
NM_002294.3(LAMP2):c.927C>T (p.Ser309=)	rs73219144	0.02702
NM_002294.3(LAMP2):c.1093+2514G>A	rs144140265	0.00404
NM_002294.3(LAMP2):c.339C>T (p.Ser113=)	rs147369153	0.00066
NM_002294.3(LAMP2):c.504C>T (p.Tyr168=)	rs150520869	0.00060
NM_002294.3(LAMP2):c.385G>A (p.Ala129Thr)	rs149276836	0.00045
NM_002294.3(LAMP2):c.586A>T (p.Thr196Ser)	rs138991195	0.00039
NM_002294.3(LAMP2):c.1142T>C (p.Val381Ala)	rs139633545	0.00026
NM_002294.3(LAMP2):c.741+11C>T	rs149155417	0.00024
NM_002294.3(LAMP2):c.1093+2450G>A	rs149783672	0.00015
NM_002294.3(LAMP2):c.1093+2478A>G	rs140936359	0.00014
NM_002294.3(LAMP2):c.1162G>T (p.Val388Leu)	rs372906565	0.00012
NM_002294.3(LAMP2):c.1093+2544A>G	rs777128122	0.00009
NM_002294.3(LAMP2):c.157C>T (p.Arg53Cys)	rs752321157	0.00009
NM_002294.3(LAMP2):c.1094-4C>T	rs768756537	0.00006
NM_002294.3(LAMP2):c.158G>A (p.Arg53His)	rs397516735	0.00005
NM_002294.3(LAMP2):c.299C>T (p.Ala100Val)	rs397516741	0.00004
NM_002294.3(LAMP2):c.929-5T>C	rs375341409	0.00004
NM_002294.3(LAMP2):c.1094-16C>T	rs772976829	0.00003
NM_002294.3(LAMP2):c.300G>A (p.Ala100=)	rs765548221	0.00003
NM_002294.3(LAMP2):c.750A>C (p.Ser250=)	rs765836082	0.00003
NM_002294.3(LAMP2):c.1125C>T (p.Phe375=)	rs746288560	0.00002
NM_002294.3(LAMP2):c.557-12C>T	rs756269189	0.00002
NM_002294.3(LAMP2):c.74G>A (p.Arg25Gln)	rs750118236	0.00002
NM_002294.3(LAMP2):c.797G>A (p.Arg266His)	rs200934351	0.00002
NM_002294.3(LAMP2):c.1191T>C (p.Phe397=)	rs752231323	0.00001
NM_002294.3(LAMP2):c.1089T>C (p.Ser363=)
NM_002294.3(LAMP2):c.742-16TCT[2]	rs730880476
NM_002294.3(LAMP2):c.742-7_742-5del	rs779710402
NM_002294.3(LAMP2):c.877C>A (p.Arg293=)	rs727503118
NM_002294.3(LAMP2):c.929-9del	rs1338648665

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