List of variants in gene TTN reported as pathogenic by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.39974-11T>G	rs758597536	0.00006
NM_001267550.2(TTN):c.53743C>T (p.Arg17915Ter)	rs753333359	0.00001
NM_001267550.2(TTN):c.31034_31035del (p.Asp10344_Tyr10345insTer)	rs2073645237
NM_001267550.2(TTN):c.55351C>T (p.Arg18451Ter)	rs1440093502

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