ClinVar Miner

List of variants in gene LAMA4 reported as likely benign for Cardiomyopathy

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.924T>C (p.His308=) rs143580603 0.00205
NM_001105206.3(LAMA4):c.1633C>T (p.Arg545Cys) rs138153075 0.00135
NM_001105206.3(LAMA4):c.674C>T (p.Ala225Val) rs149615862 0.00052
NM_001105206.3(LAMA4):c.641G>A (p.Arg214His) rs139146419 0.00044
NM_001105206.3(LAMA4):c.3054G>T (p.Leu1018Phe) rs183262122 0.00040
NM_001105206.3(LAMA4):c.668G>A (p.Arg223His) rs200017155 0.00019
NM_001105206.3(LAMA4):c.3147T>C (p.Ser1049=) rs149203646 0.00015
NM_001105206.3(LAMA4):c.873C>T (p.Ile291=) rs141611768 0.00014
NM_001105206.3(LAMA4):c.1821G>A (p.Lys607=) rs374481199 0.00010
NM_001105206.3(LAMA4):c.167C>T (p.Ala56Val) rs372763422 0.00006
NM_001105206.3(LAMA4):c.2226C>T (p.Asn742=) rs530906240 0.00004
NM_001105206.3(LAMA4):c.513C>T (p.Pro171=) rs140249081 0.00004
NM_001105206.3(LAMA4):c.572G>A (p.Gly191Glu) rs782010849 0.00003
NM_001105206.3(LAMA4):c.1854G>A (p.Gln618=) rs587781014 0.00001
NM_001105206.3(LAMA4):c.222C>G (p.Thr74=) rs1784629877 0.00001
NM_001105206.3(LAMA4):c.4476-10C>A rs899288475 0.00001
NM_001105206.3(LAMA4):c.5004G>A (p.Leu1668=) rs781868926 0.00001
NM_001105206.3(LAMA4):c.633T>C (p.Asn211=) rs782555068 0.00001
NM_001105206.3(LAMA4):c.4914C>T (p.Thr1638=) rs1554324464
NM_001105206.3(LAMA4):c.738C>T (p.Gly246=) rs782462144

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