ClinVar Miner

List of variants in gene LAMA4 reported as uncertain significance by Stanford Center for Inherited Cardiovascular Disease,Stanford University

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Total variants: 11
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HGVS dbSNP
NM_001105206.3(LAMA4):c.1277T>C (p.Met426Thr) rs200112094
NM_001105206.3(LAMA4):c.1475T>A (p.Leu492His) rs3752579
NM_001105206.3(LAMA4):c.1673C>T (p.Ala558Val) rs137893207
NM_001105206.3(LAMA4):c.1961C>T (p.Ala654Val) rs782806847
NM_001105206.3(LAMA4):c.2417G>A (p.Arg806Gln) rs1554334150
NM_001105206.3(LAMA4):c.355G>A (p.Gly119Arg) rs147016335
NM_001105206.3(LAMA4):c.371G>A (p.Gly124Glu) rs1562733361
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr) rs141261442
NM_001105206.3(LAMA4):c.5206+1G>A rs368035482
NM_001105206.3(LAMA4):c.59C>T (p.Ala20Val) rs1060500981
NM_001105206.3(LAMA4):c.874G>A (p.Glu292Lys) rs781838464

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