List of variants in gene combination LOC126806421, TTN reported as 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.96310+2T>G	rs794729303
NM_001267550.2(TTN):c.96669G>A (p.Trp32223Ter)	rs2154143423
NM_001267550.2(TTN):c.96849del (p.Gly32284fs)	rs2154143293

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