List of variants in gene combination LOC126806429, TTN reported as uncertain significance for Cardiomyopathy

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.19770A>G (p.Thr6590=)	rs775289296	0.00004
NM_001267550.2(TTN):c.19744C>T (p.Arg6582Ter)	rs794727829
NM_001267550.2(TTN):c.20148G>A (p.Met6716Ile)

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