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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_002294.3(LAMP2):c.1075C>T (p.Gln359Ter)	rs1057517940
NM_002294.3(LAMP2):c.1094-2A>G	rs2147273254
NM_002294.3(LAMP2):c.183+5G>A	rs730880479
NM_002294.3(LAMP2):c.184-1G>T	rs1064796635
NM_002294.3(LAMP2):c.1A>G (p.Met1Val)
NM_002294.3(LAMP2):c.1A>T (p.Met1Leu)	rs1556124149
NM_002294.3(LAMP2):c.659dup (p.Gly221fs)	rs1556101640
NM_002294.3(LAMP2):c.669T>G (p.Tyr223Ter)	rs1602535807
NM_002294.3(LAMP2):c.834del (p.Ile279fs)	rs1602534666
NM_002294.3(LAMP2):c.854_859del (p.Val285_Phe286del)
NM_002294.3(LAMP2):c.864+3_864+6del	rs397516751
NM_002294.3(LAMP2):c.929-1G>A	rs727504262
NM_002294.3(LAMP2):c.929-2A>G	rs1556092556

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