ClinVar Miner

List of variants in gene combination LOC126806430, TTN reported as likely benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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.18659G>C (p.Cys6220Ser)	rs191692293	0.00188
NM_001267550.2(TTN):c.18470T>C (p.Ile6157Thr)	rs371882162	0.00009

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