List of variants in gene combination LOC126806433, TTN reported as likely pathogenic for not provided

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.6959G>A (p.Arg2320His)	rs374615369	0.00008
NM_001267550.2(TTN):c.7057+2dup	rs765019023	0.00002
NM_001267550.2(TTN):c.6820C>T (p.Gln2274Ter)	rs145649088
NM_001267550.2(TTN):c.7439del (p.Tyr2479_Leu2480insTer)

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