List of variants in gene TTN reported as uncertain significance by Centogene AG - the Rare Disease Company

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.34435G>C (p.Glu11479Gln)	rs1298237270	0.00001
NM_001267550.2(TTN):c.82019T>A (p.Ile27340Lys)	rs371592971	0.00001
NM_001267550.2(TTN):c.38523del (p.Lys12841fs)	rs1457702153
NM_001267550.2(TTN):c.82720C>T (p.Pro27574Ser)	rs2154161353

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