ClinVar Miner

List of variants in gene TTN reported as uncertain significance by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.97441G>A (p.Gly32481Arg)	rs111616037	0.00004
NM_001267550.2(TTN):c.1364C>T (p.Thr455Met)	rs368121196

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