List of variants in gene TTN reported as pathogenic by Clinical Genetics, Academic Medical Center

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.85090C>T (p.Arg28364Ter)	rs770038577	0.00001
NM_001267550.2(TTN):c.102510G>A (p.Trp34170Ter)	rs1559033550
NM_001267550.2(TTN):c.53918del (p.Gly17973fs)	rs1486129583
NM_001267550.2(TTN):c.86640C>A (p.Tyr28880Ter)	rs794729298
NM_001267550.2(TTN):c.98990-1G>T	rs796111471

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