ClinVar Miner

List of variants in gene combination LAMA4, LOC126859766 reported as likely benign for cardiomyopathy

Included ClinVar conditions (559):
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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.2810A>G (p.Glu937Gly) rs35605307 0.00349
NM_001105206.3(LAMA4):c.2850G>A (p.Pro950=) rs368741631 0.00014
NM_001105206.3(LAMA4):c.2718C>T (p.Tyr906=) rs530825191 0.00011
NM_001105206.3(LAMA4):c.2769C>T (p.Pro923=) rs782151816 0.00009
NM_001105206.3(LAMA4):c.2901G>A (p.Ser967=) rs148096716 0.00005
NM_001105206.3(LAMA4):c.2668-13C>A rs782264610 0.00001
NM_001105206.3(LAMA4):c.2724T>C (p.Tyr908=) rs782740441 0.00001
NM_001105206.3(LAMA4):c.2745G>A (p.Val915=) rs1554333214 0.00001
NM_001105206.3(LAMA4):c.2813+7T>C rs370599915 0.00001
NM_001105206.3(LAMA4):c.2668-4T>G rs1554333244
NM_001105206.3(LAMA4):c.2668-6T>C rs782482637
NM_001105206.3(LAMA4):c.2694A>C (p.Ala898=)
NM_001105206.3(LAMA4):c.2712G>A (p.Leu904=)
NM_001105206.3(LAMA4):c.2715A>G (p.Val905=)
NM_001105206.3(LAMA4):c.2772C>T (p.Val924=)
NM_001105206.3(LAMA4):c.2790C>T (p.Tyr930=)
NM_001105206.3(LAMA4):c.2813+13C>A rs782514628
NM_001105206.3(LAMA4):c.2813+15T>G
NM_001105206.3(LAMA4):c.2813+16G>T
NM_001105206.3(LAMA4):c.2814-5A>C
NM_001105206.3(LAMA4):c.2859T>C (p.Ser953=)
NM_001105206.3(LAMA4):c.2874A>G (p.Glu958=) rs1779650229
NM_001105206.3(LAMA4):c.2917C>T (p.Leu973=) rs1554332949

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