ClinVar Miner

List of variants in gene LAMP2 reported as likely benign by GeneDx

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Total variants: 37
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HGVS dbSNP
NM_001122606.1(LAMP2):c.1094-2739T>C rs752231323
NM_001122606.1(LAMP2):c.1094-2791C>T rs747301460
NM_001122606.1(LAMP2):c.1094-2840C>T rs768756537
NM_002294.3(LAMP2):c.*15T>C rs376806600
NM_002294.3(LAMP2):c.1142T>C (p.Val381Ala) rs139633545
NM_002294.3(LAMP2):c.299C>T (p.Ala100Val) rs397516741
NM_002294.3(LAMP2):c.517G>A (p.Val173Ile) rs141574558
NM_002294.3(LAMP2):c.586A>T (p.Thr196Ser) rs138991195
NM_002294.3(LAMP2):c.65-13T>A rs727503121
NM_002294.3(LAMP2):c.661G>A (p.Gly221Arg) rs145169006
NM_002294.3(LAMP2):c.742-7_742-5del rs779710402
NM_013995.2(LAMP2):c.-32_-24GTCGCCGCC[3] rs193922648
NM_013995.2(LAMP2):c.-38G>C rs1354020682
NM_013995.2(LAMP2):c.1093+17C>T rs1057521759
NM_013995.2(LAMP2):c.1093+9C>G rs371259269
NM_013995.2(LAMP2):c.150C>T (p.Phe50=) rs1057521701
NM_013995.2(LAMP2):c.157C>T (p.Arg53Cys) rs752321157
NM_013995.2(LAMP2):c.204C>G (p.Asp68Glu) rs376215728
NM_013995.2(LAMP2):c.340G>A (p.Val114Ile) rs377652722
NM_013995.2(LAMP2):c.385G>A (p.Ala129Thr) rs149276836
NM_013995.2(LAMP2):c.398-4A>G rs1057523043
NM_013995.2(LAMP2):c.504C>T (p.Tyr168=) rs150520869
NM_013995.2(LAMP2):c.557-129dup rs775935754
NM_013995.2(LAMP2):c.557-251G>T rs148242561
NM_013995.2(LAMP2):c.605A>C (p.His202Pro) rs730880475
NM_013995.2(LAMP2):c.64+16C>G rs780307352
NM_013995.2(LAMP2):c.64+20C>G rs1346805727
NM_013995.2(LAMP2):c.65-20A>T rs773064698
NM_013995.2(LAMP2):c.65-3C>T rs769801659
NM_013995.2(LAMP2):c.771T>C (p.Asn257=) rs138435481
NM_013995.2(LAMP2):c.865-13C>T rs760238519
NM_013995.2(LAMP2):c.865-242C>A rs146283621
NM_013995.2(LAMP2):c.865-9T>C rs1057522838
NM_013995.2(LAMP2):c.877C>A (p.Arg293=) rs727503118
NM_013995.2(LAMP2):c.907A>G (p.Met303Val) rs768369360
NM_013995.2(LAMP2):c.929-126G>A rs7888393
NM_013995.2(LAMP2):c.972C>G (p.Pro324=) rs1229203142

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