ClinVar Miner

List of variants in gene combination LOC126806423, TTN reported as likely benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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.67542T>G (p.Thr22514=)	rs72646876	0.00048
NM_001267550.2(TTN):c.67833C>T (p.Tyr22611=)	rs375538420	0.00027

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