List of variants in gene combination C10orf105, CDH23 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.3369+12G>A	rs187975106	0.00061
NM_022124.6(CDH23):c.4203C>T (p.Thr1401=)	rs202166096	0.00058
NM_022124.6(CDH23):c.3895G>A (p.Val1299Ile)	rs201610096	0.00027
NM_022124.6(CDH23):c.3431-6A>T	rs377614198	0.00018
NM_022124.6(CDH23):c.3480G>T (p.Met1160Ile)	rs111033519	0.00010
NM_022124.6(CDH23):c.3352G>A (p.Gly1118Ser)	rs562052236	0.00009
NM_022124.6(CDH23):c.3331G>A (p.Val1111Ile)	rs397517321	0.00006
NM_022124.6(CDH23):c.3408T>A (p.Arg1136=)	rs1223980355	0.00001
NM_022124.6(CDH23):c.3438T>C (p.His1146=)	rs775496154	0.00001
NM_022124.6(CDH23):c.4128G>C (p.Leu1376=)	rs773827025	0.00001
NM_022124.6(CDH23):c.3486G>T (p.Gly1162=)	rs397517324

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