ClinVar Miner

List of variants in gene combination LOC126806430, 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.18390A>T (p.Thr6130=)	rs66523653	0.01518
NM_001267550.2(TTN):c.18719G>A (p.Arg6240Gln)	rs761993856	0.00004

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