List of variants in gene combination LOC126806423, TTN reported as likely pathogenic for Primary dilated cardiomyopathy

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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.67495C>T (p.Arg22499Ter)	rs574660186	0.00004
NM_001267550.2(TTN):c.67637-2A>G	rs869025550
NM_001267550.2(TTN):c.67875_67876dup (p.Lys22626fs)
NM_001267550.2(TTN):c.67900G>T (p.Gly22634Ter)
NM_001267550.2(TTN):c.68172T>G (p.Tyr22724Ter)
NM_001267550.2(TTN):c.68195C>A (p.Ser22732Ter)	rs727505352

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