ClinVar Miner

List of variants in gene combination LOC126806433, TTN reported as uncertain significance by Institute of Human Genetics, University of Leipzig Medical Center

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.6959G>A (p.Arg2320His)	rs374615369	0.00008
NM_001267550.2(TTN):c.7057+1G>A	rs763909866	0.00002

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