List of variants in gene combination LOC126806421, TTN reported as likely pathogenic for Cardiovascular phenotype

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.96233_96236delinsCCT (p.Tyr32078fs)	rs1553518529
NM_001267550.2(TTN):c.96260_96279dup (p.Lys32094fs)	rs2154143867
NM_001267550.2(TTN):c.96477C>A (p.Cys32159Ter)
NM_001267550.2(TTN):c.96669G>A (p.Trp32223Ter)	rs2154143423
NM_001267550.2(TTN):c.96680_96684del (p.Leu32227fs)
NM_001267550.2(TTN):c.96682dup (p.Tyr32228fs)	rs2154143418
NM_001267550.2(TTN):c.96697C>T (p.Arg32233Ter)	rs781171206
NM_001267550.2(TTN):c.96853del (p.Val32285fs)

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