ClinVar Miner

List of variants in gene combination C10orf105, CDH23 reported as likely benign for Inborn genetic diseases

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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_022124.6(CDH23):c.3331G>A (p.Val1111Ile)	rs397517321	0.00006
NM_022124.6(CDH23):c.3695A>G (p.Gln1232Arg)	rs776158881	0.00002

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