List of variants in gene LAMP2 reported as likely benign for Hypertrophic cardiomyopathy

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_002294.3(LAMP2):c.*4579A>G	rs42885	0.62750
NM_002294.3(LAMP2):c.156A>T (p.Val52=)	rs12097	0.39324
NM_002294.3(LAMP2):c.*5038A>G	rs2748	0.28585
NM_002294.3(LAMP2):c.*1314T>C	rs5957381	0.09876
NM_002294.3(LAMP2):c.*297A>C	rs8160	0.09815
NM_002294.3(LAMP2):c.*3248G>A	rs5957380	0.09812
NM_002294.3(LAMP2):c.*4671C>T	rs1045953	0.09801
NM_002294.3(LAMP2):c.*486A>G	rs5957383	0.09784
NM_002294.3(LAMP2):c.*2395A>G	rs10127185	0.09686
NM_002294.3(LAMP2):c.*2261A>G	rs12395643	0.09416
NM_002294.3(LAMP2):c.*2460A>G	rs10127182	0.08629
NM_002294.3(LAMP2):c.*2195T>C	rs13441024	0.08473
NM_002294.3(LAMP2):c.*1096T>C	rs5957382	0.06824
NM_002294.3(LAMP2):c.*1071G>T	rs2285548	0.03391
NM_002294.3(LAMP2):c.*1589A>G	rs73612906	0.03180
NM_002294.3(LAMP2):c.927C>T (p.Ser309=)	rs73219144	0.02702
NM_002294.3(LAMP2):c.*205C>T	rs41300191	0.02502
NM_002294.3(LAMP2):c.*4562A>G	rs142200759	0.01528
NM_002294.3(LAMP2):c.*1617C>T	rs141881232	0.01521
NM_002294.3(LAMP2):c.*2746A>G	rs3827478	0.01396
NM_002294.3(LAMP2):c.*2162G>A	rs767123866	0.00966
NM_002294.3(LAMP2):c.*5048A>T	rs113285013	0.00807
NM_002294.3(LAMP2):c.1093+2514G>A	rs144140265	0.00404
NM_002294.3(LAMP2):c.586A>T (p.Thr196Ser)	rs138991195	0.00039
NM_002294.3(LAMP2):c.*1701dup	rs373005118
NM_002294.3(LAMP2):c.*2148AT[9]	rs753399289
NM_002294.3(LAMP2):c.*3031dup	rs113549733
NM_002294.3(LAMP2):c.*3459GTT[3]	rs199705754

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