List of variants in gene combination LOC101927055, 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.3780T>G (p.Tyr1260Ter)
NM_001267550.2(TTN):c.3937A>T (p.Lys1313Ter)
NM_001267550.2(TTN):c.4027C>T (p.Gln1343Ter)	rs727503697
NM_001267550.2(TTN):c.4724_4728del (p.Met1575fs)	rs756433029

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