List of variants in gene combination LOC126806430, TTN reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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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.18663A>C (p.Glu6221Asp)	rs369544339	0.00010
NM_001267550.2(TTN):c.18173G>A (p.Arg6058His)	rs376012117	0.00004
NM_001267550.2(TTN):c.18646G>A (p.Val6216Met)	rs369242073	0.00003
NM_001267550.2(TTN):c.18767T>G (p.Leu6256Arg)	rs780526976	0.00002
NM_001267550.2(TTN):c.18628del (p.Glu6209_Val6210insTer)
NM_001267550.2(TTN):c.18923C>A (p.Ser6308Tyr)

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