ClinVar Miner

List of variants in gene LAMP2 reported as uncertain significance by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 26
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HGVS dbSNP
NM_001122606.1(LAMP2):c.(?_1094)_(1236_?)del
NM_002294.2(LAMP2):c.-10C>T rs201209341
NM_002294.2(LAMP2):c.-4G>A rs200297370
NM_002294.2(LAMP2):c.-4G>C rs200297370
NM_002294.2(LAMP2):c.1117G>A (p.Asp373Asn) rs727503117
NM_002294.2(LAMP2):c.1142T>C (p.Val381Ala) rs139633545
NM_002294.2(LAMP2):c.1193T>C (p.Ile398Thr) rs727504625
NM_002294.2(LAMP2):c.1211A>T (p.His404Leu) rs727504957
NM_002294.2(LAMP2):c.158G>A (p.Arg53His) rs397516735
NM_002294.2(LAMP2):c.184-7C>G rs397516737
NM_002294.2(LAMP2):c.214G>A (p.Val72Met) rs778193991
NM_002294.2(LAMP2):c.32G>T (p.Gly11Val) rs3180515
NM_002294.2(LAMP2):c.371C>T (p.Thr124Ile) rs397516744
NM_002294.2(LAMP2):c.472A>G (p.Thr158Ala) rs138374063
NM_002294.2(LAMP2):c.517G>A (p.Val173Ile) rs141574558
NM_002294.2(LAMP2):c.56T>G (p.Leu19Arg) rs397516745
NM_002294.2(LAMP2):c.602T>C (p.Ile201Thr) rs876657844
NM_002294.2(LAMP2):c.610A>C (p.Thr204Pro) rs876657845
NM_002294.2(LAMP2):c.65-13T>A rs727503121
NM_002294.2(LAMP2):c.824A>G (p.Asn275Ser) rs397516747
NM_002294.2(LAMP2):c.842A>G (p.Tyr281Cys) rs397516748
NM_002294.2(LAMP2):c.845T>G (p.Leu282Arg) rs397516749
NM_002294.2(LAMP2):c.865-3C>A rs397516753
NM_013995.2(LAMP2):c.1106C>T (p.Ser369Leu) rs765143363
NM_013995.2(LAMP2):c.1195G>A
NM_013995.2(LAMP2):c.1222C>G (p.Gln408Glu) rs876657846

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