ClinVar Miner

List of variants reported as not provided for TTN-Related Disorders

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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.80701A>G (p.Ile26901Val) rs201562505 0.00102
NM_001267550.2(TTN):c.18745G>A (p.Asp6249Asn) rs201263441 0.00021
NM_001267550.2(TTN):c.106537A>G (p.Lys35513Glu) rs551063889 0.00006
NM_001267550.2(TTN):c.92905C>T (p.Arg30969Trp) rs754767262 0.00001
NM_001267550.2(TTN):c.13025A>G (p.Lys4342Arg) rs2082249607
NM_001267550.2(TTN):c.13942G>A (p.Glu4648Lys) rs1553936042
NM_001267550.2(TTN):c.70475G>A (p.Cys23492Tyr)

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