ClinVar Miner

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

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Total variants: 13
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HGVS dbSNP
NM_001105206.3(LAMA4):c.1633C>T (p.Arg545Cys) rs138153075
NM_001105206.3(LAMA4):c.1821G>A (p.Lys607=) rs374481199
NM_001105206.3(LAMA4):c.2226C>T (p.Asn742=) rs530906240
NM_001105206.3(LAMA4):c.2745G>A (p.Val915=) rs1554333214
NM_001105206.3(LAMA4):c.2917C>T (p.Leu973=) rs1554332949
NM_001105206.3(LAMA4):c.3147T>C (p.Ser1049=) rs149203646
NM_001105206.3(LAMA4):c.486T>C (p.Ala162=) rs397516734
NM_001105206.3(LAMA4):c.4914C>T (p.Thr1638=) rs1554324464
NM_001105206.3(LAMA4):c.513C>T (p.Pro171=) rs140249081
NM_001105206.3(LAMA4):c.633T>C (p.Asn211=) rs782555068
NM_001105206.3(LAMA4):c.641G>A (p.Arg214His) rs139146419
NM_001105206.3(LAMA4):c.738C>T (p.Gly246=) rs782462144
NM_001105206.3(LAMA4):c.924T>C (p.His308=) rs143580603

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