List of variants in gene combination LOC126806429, TTN reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.20275+109G>A	rs114742263	0.02044
NM_001267550.2(TTN):c.19976C>T (p.Thr6659Met)	rs16866475	0.01294
NM_001267550.2(TTN):c.20147T>A (p.Met6716Lys)	rs28626194	0.00641
NM_001267550.2(TTN):c.20275+136C>T	rs79057558	0.00465

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