Variants in gene LAMP2 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 11

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HGVS	dbSNP	gnomAD frequency
NM_002294.3(LAMP2):c.1093+2514G>A	rs144140265	0.00404
NM_002294.3(LAMP2):c.385G>A (p.Ala129Thr)	rs149276836	0.00045
NM_002294.3(LAMP2):c.-10C>T	rs201209341	0.00028
NM_002294.3(LAMP2):c.1142T>C (p.Val381Ala)	rs139633545	0.00026
NM_002294.3(LAMP2):c.1093+2544A>G	rs777128122	0.00009
NM_002294.3(LAMP2):c.158G>A (p.Arg53His)	rs397516735	0.00005
NM_002294.3(LAMP2):c.-7C>T	rs762305947	0.00004
NM_002294.3(LAMP2):c.929-5T>C	rs375341409	0.00004
NM_002294.3(LAMP2):c.183T>C (p.Tyr61=)	rs397516736	0.00002
NM_002294.3(LAMP2):c.-4G>C	rs200297370
NM_002294.3(LAMP2):c.865-8del	rs746330494

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