ClinVar Miner

List of variants in gene combination LOC126806429, TTN reported as likely benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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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.20175A>G (p.Ile6725Met)	rs146627500	0.00104
NM_001267550.2(TTN):c.19881G>A (p.Ser6627=)	rs371495674	0.00012

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