List of variants in gene combination LOC126806420, TTN reported as likely pathogenic by GeneDx

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.100127_100151dup (p.Ile33385fs)	rs1553503113
NM_001267550.2(TTN):c.100161del (p.Ser33388fs)	rs2468648655
NM_001267550.2(TTN):c.100281C>G (p.Tyr33427Ter)	rs373085562
NM_001267550.2(TTN):c.99780_99812del (p.Arg33261_Gln33271del)	rs2468670396
NM_001267550.2(TTN):c.99919_99920dup (p.Ala33308fs)	rs886043854

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