List of variants reported as uncertain significance for Primary dilated cardiomyopathy by Center for Human Genetics, University of Leuven

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001032283.3(TMPO):c.370C>T (p.Leu124Phe)	rs375619307	0.00002
NM_001267550.2(TTN):c.51436+1G>A	rs761807131	0.00001
NM_005751.5(AKAP9):c.2478A>G (p.Ile826Met)	rs777349648	0.00001
NM_201596.3(CACNB2):c.1276G>A (p.Ala426Thr)	rs1336353571	0.00001
NM_000257.4(MYH7):c.1128C>A (p.Asp376Glu)	rs2231126
NM_004588.5(SCN2B):c.332C>T (p.Ser111Leu)	rs868793059
NM_172201.2(KCNE2):c.285G>T (p.Lys95Asn)	rs1555837113

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