ClinVar Miner

List of variants in gene TTN reported as benign by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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.60232G>A (p.Val20078Met)	rs77351975	0.00719
NM_001267550.2(TTN):c.97193-16T>G	rs371317486	0.00011

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