ClinVar Miner

List of variants in gene TTN reported as uncertain significance by Division of Human Genetics, Children's Hospital of Philadelphia

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.98960C>T (p.Ser32987Phe)	rs746380940	0.00015
NM_001267550.2(TTN):c.40558+1G>A	rs368219776	0.00004

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