List of variants in gene combination LOC126806429, TTN reported as likely pathogenic

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.19715-1G>A	rs767658044	0.00003
NM_001267550.2(TTN):c.20107C>T (p.Arg6703Ter)	rs2079499416	0.00001
NM_001267550.2(TTN):c.19744C>T (p.Arg6582Ter)	rs794727829
NM_001267550.2(TTN):c.20008del (p.Phe6669_Val6670insTer)

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