List of variants in gene CDH23 reported as uncertain significance for Optic atrophy

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.5647A>C (p.Asn1883His)	rs747488431	0.00023
NM_022124.6(CDH23):c.9979G>A (p.Ala3327Thr)	rs200733236	0.00006
NM_022124.6(CDH23):c.1153A>T (p.Met385Leu)	rs772474417	0.00001
NM_022124.6(CDH23):c.7762G>A (p.Glu2588Lys)

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