ClinVar Miner

List of variants in gene TTN reported as uncertain significance by Muscle and Diseases Team, Institut de Génétique et Biologie Moléculaire et Cellulaire

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.106374G>A (p.Lys35458=)	rs2154132585
NM_001267550.2(TTN):c.35713+1G>A	rs2066160245

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