ClinVar Miner

List of variants in gene LAMA4 reported as uncertain significance for Cardiomyopathy

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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519 0.00067
NM_001105206.3(LAMA4):c.*1C>T rs148811960 0.00048
NM_001105206.3(LAMA4):c.3054G>T (p.Leu1018Phe) rs183262122 0.00040
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr) rs141261442 0.00022
NM_001105206.3(LAMA4):c.4493G>A (p.Arg1498His) rs147556641 0.00014
NM_001105206.3(LAMA4):c.1673C>T (p.Ala558Val) rs137893207 0.00013
NM_001105206.3(LAMA4):c.3283-3C>G rs374159760 0.00011
NM_001105206.3(LAMA4):c.1390C>G (p.His464Asp) rs151119304 0.00010
NM_001105206.3(LAMA4):c.4405G>A (p.Ala1469Thr) rs727504595 0.00008
NM_001105206.3(LAMA4):c.3834G>A (p.Gly1278=) rs141988342 0.00006
NM_001105206.3(LAMA4):c.5437G>A (p.Gly1813Ser) rs142048329 0.00006
NM_001105206.3(LAMA4):c.928C>G (p.His310Asp) rs374968791 0.00006
NM_001105206.3(LAMA4):c.1385G>A (p.Arg462Gln) rs781977997 0.00004
NM_001105206.3(LAMA4):c.572G>A (p.Gly191Glu) rs782010849 0.00003
NM_001105206.3(LAMA4):c.652G>A (p.Gly218Arg) rs781829741 0.00003
NM_001105206.3(LAMA4):c.1507G>A (p.Glu503Lys) rs782568868 0.00002
NM_001105206.3(LAMA4):c.1455G>T (p.Leu485Phe) rs782305599 0.00001
NM_001105206.3(LAMA4):c.1726C>G (p.Leu576Val) rs782074007 0.00001
NM_001105206.3(LAMA4):c.2195G>A (p.Gly732Glu) rs781889038 0.00001
NM_001105206.3(LAMA4):c.4111A>C (p.Ile1371Leu) rs974775253 0.00001
NM_001105206.3(LAMA4):c.837C>T (p.Asp279=) rs782335744 0.00001
NM_001105206.3(LAMA4):c.1140C>T (p.His380=) rs782378476
NM_001105206.3(LAMA4):c.1842C>G (p.Asn614Lys) rs782388698
NM_001105206.3(LAMA4):c.3095_3103del (p.Ser1032_Pro1034del) rs1779575645
NM_001105206.3(LAMA4):c.3110+10A>C rs1554332565
NM_001105206.3(LAMA4):c.3234A>G (p.Glu1078=) rs1779530897
NM_001105206.3(LAMA4):c.4606G>C (p.Gly1536Arg) rs1378834238
NM_001105206.3(LAMA4):c.5269C>T (p.Pro1757Ser) rs782001026

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