List of variants in gene combination LOC126806433, TTN reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.6950G>A (p.Arg2317His)	rs764882950	0.00006
NM_001267550.2(TTN):c.6866T>G (p.Ile2289Ser)	rs200440412	0.00001
NM_001267550.2(TTN):c.6890G>A (p.Gly2297Glu)
NM_001267550.2(TTN):c.7330+5G>A	rs869025547

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