List of variants in gene TTN reported as uncertain significance by Institute of Human Genetics, University of Leipzig Medical Center

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.54796G>T (p.Ala18266Ser)	rs199837769	0.00013
NM_001267550.2(TTN):c.104261C>T (p.Ala34754Val)	rs727505020	0.00006
NM_001267550.2(TTN):c.2447T>C (p.Phe816Ser)	rs2093121464
NM_001267550.2(TTN):c.28383del (p.Gly9462fs)	rs2154295037
NM_001267550.2(TTN):c.38424del (p.Lys12809fs)	rs1553775991
NM_001267550.2(TTN):c.49621G>T (p.Glu16541Ter)	rs2056671421
NM_001267550.2(TTN):c.60988T>C (p.Phe20330Leu)	rs2050031384

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