ClinVar Miner

List of variants in gene TTN reported as uncertain significance for left ventricular noncompaction 2

Included ClinVar conditions (1):

Left ventricular noncompaction 2

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.104978C>T (p.Thr34993Met)	rs368945564	0.00004
NM_001267550.2(TTN):c.42872C>T (p.Ala14291Val)	rs746486506	0.00001

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