ClinVar Miner

List of variants in gene LAMP2 reported as likely benign for not specified

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Gene type:
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Total variants: 49
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HGVS dbSNP
NM_001122606.1(LAMP2):c.1093+2589C>T rs377303143
NM_001122606.1(LAMP2):c.1094-2682T>C rs376806600
NM_001122606.1(LAMP2):c.1094-2739T>C rs752231323
NM_001122606.1(LAMP2):c.1094-2788T>C rs139633545
NM_001122606.1(LAMP2):c.1094-2791C>T rs747301460
NM_001122606.1(LAMP2):c.1094-2840C>T rs768756537
NM_001122606.1(LAMP2):c.1170A>C (p.Ile390=) rs397516587
NM_013995.2(LAMP2):c.-32_-24GTCGCCGCC[1] 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.1107G>A (p.Ser369=) rs149783672
NM_013995.2(LAMP2):c.1171G>A (p.Val391Ile) rs144140265
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.276C>T (p.Phe92=) rs754577706
NM_013995.2(LAMP2):c.277G>A (p.Gly93Arg) rs727504953
NM_013995.2(LAMP2):c.299C>T (p.Ala100Val) rs397516741
NM_013995.2(LAMP2):c.333T>C (p.Ile111=) rs397516742
NM_013995.2(LAMP2):c.339C>T (p.Ser113=) rs147369153
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.398-7T>C rs876657483
NM_013995.2(LAMP2):c.42C>T (p.Leu14=) rs727503122
NM_013995.2(LAMP2):c.504C>T (p.Tyr168=) rs150520869
NM_013995.2(LAMP2):c.517G>A (p.Val173Ile) rs141574558
NM_013995.2(LAMP2):c.586A>T (p.Thr196Ser) rs138991195
NM_013995.2(LAMP2):c.591G>A (p.Val197=) rs201030806
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.65-13T>A rs727503121
NM_013995.2(LAMP2):c.65-20A>T rs773064698
NM_013995.2(LAMP2):c.65-3C>T rs769801659
NM_013995.2(LAMP2):c.657A>G (p.Glu219=) rs876657484
NM_013995.2(LAMP2):c.661G>A (p.Gly221Arg) rs145169006
NM_013995.2(LAMP2):c.672A>G (p.Ser224=) rs397516746
NM_013995.2(LAMP2):c.742-7_742-5del rs779710402
NM_013995.2(LAMP2):c.755T>G (p.Ile252Ser) rs141541387
NM_013995.2(LAMP2):c.771T>C (p.Asn257=) rs138435481
NM_013995.2(LAMP2):c.813A>G (p.Leu271=) rs876657485
NM_013995.2(LAMP2):c.855C>T (p.Val285=) rs397516750
NM_013995.2(LAMP2):c.865-13C>T rs760238519
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.972C>G (p.Pro324=) rs1229203142

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