ClinVar Miner

List of variants in gene combination LOC126806423, TTN reported as 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.67637-17T>C	rs2288571	0.24363
NM_001267550.2(TTN):c.68217T>C (p.His22739=)	rs10497517	0.09829

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