ClinVar Miner

List of variants reported as uncertain significance for Dilated cardiomyopathy 1G by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.40558+1G>A rs368219776 0.00004
NM_001267550.2(TTN):c.67147G>A (p.Gly22383Arg) rs372388682 0.00004
NM_001267550.2(TTN):c.86024C>T (p.Pro28675Leu) rs766419568 0.00002
NM_001267550.2(TTN):c.16288C>T (p.Arg5430Ter) rs772235481 0.00001
NM_001267550.2(TTN):c.32471-1G>A rs371725574 0.00001
NM_001267550.2(TTN):c.82405C>G (p.Pro27469Ala) rs769678793 0.00001
NM_001267550.2(TTN):c.107387A>C (p.Glu35796Ala) rs1553478042
NM_001267550.2(TTN):c.22982A>C (p.Asn7661Thr) rs2078278433
NM_001267550.2(TTN):c.39985C>G (p.Pro13329Ala)
NM_001267550.2(TTN):c.54613A>G (p.Lys18205Glu)
NM_001267550.2(TTN):c.57103T>G (p.Trp19035Gly)
NM_001267550.2(TTN):c.61054G>A (p.Gly20352Arg)
NM_001267550.2(TTN):c.718G>T (p.Val240Phe)
NM_001267550.2(TTN):c.84554G>A (p.Arg28185Gln)
NM_001267550.2(TTN):c.85853G>A (p.Gly28618Glu)
NM_001267550.2(TTN):c.90890T>A (p.Phe30297Tyr) rs786205537
NM_001267550.2(TTN):c.95342G>A (p.Arg31781Gln) rs748984928
NM_001267550.2(TTN):c.99506G>A (p.Gly33169Asp)

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