ClinVar Miner

List of variants in gene combination C10orf105, CDH23 reported by Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.3739C>T (p.Arg1247Cys)	rs202204597	0.00003
NM_022124.6(CDH23):c.3448T>C (p.Phe1150Leu)
NM_022124.6(CDH23):c.3616C>A (p.Pro1206Thr)
NM_022124.6(CDH23):c.3715+2T>A

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