List of variants in gene combination LOC126806433, TTN reported as likely benign 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.7061G>A (p.Arg2354His)	rs75031300	0.00287
NM_001267550.2(TTN):c.6945A>G (p.Thr2315=)	rs879103814	0.00002
NM_001267550.2(TTN):c.7107G>A (p.Glu2369=)	rs2154344970
NM_001267550.2(TTN):c.7158C>T (p.Gly2386=)	rs780363319
NM_001267550.2(TTN):c.7413T>A (p.Pro2471=)

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