List of variants in gene combination LOC126806422, 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.69645del (p.Ser23215fs)	rs794729333
NM_001267550.2(TTN):c.69835_69844del (p.Glu23278_His23279insTer)	rs2154172889
NM_001267550.2(TTN):c.70128del (p.Thr23377fs)	rs1553614521
NM_001267550.2(TTN):c.70383_70386del (p.Ile23461fs)
NM_001267550.2(TTN):c.70501G>T (p.Glu23501Ter)	rs1709809170
NM_001267550.2(TTN):c.70571_70572dup (p.Glu23525fs)	rs1709775754

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