ClinVar Miner

List of variants in gene LAMP2 reported as uncertain significance for Cardiovascular phenotype

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Total variants: 10
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HGVS dbSNP
NM_002294.2(LAMP2):c.1069G>A (p.Val357Met) rs886038907
NM_002294.2(LAMP2):c.1091C>T (p.Thr364Ile) rs183781327
NM_002294.2(LAMP2):c.1142T>C (p.Val381Ala) rs139633545
NM_002294.2(LAMP2):c.183T>C (p.Tyr61=) rs397516736
NM_002294.2(LAMP2):c.320C>G (p.Ser107Cys) rs730880497
NM_002294.2(LAMP2):c.64+4delAinsGT rs1556123906
NM_002294.2(LAMP2):c.73C>T (p.Arg25Trp) rs730880478
NM_002294.2(LAMP2):c.741G>T (p.Lys247Asn) rs1556101296
NM_002294.2(LAMP2):c.864+5G>T rs1352584474
NM_002294.2(LAMP2):c.887T>G (p.Leu296Arg) rs730880486

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