List of variants in gene combination CDH23, PSAP reported as benign by Eurofins Ntd Llc (ga)

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_002778.4(PSAP):c.1351-14A>G	rs4747203	0.34512
NM_022124.6(CDH23):c.9873G>A (p.Thr3291=)	rs2290021	0.08719
NM_022124.6(CDH23):c.9758A>C (p.Asp3253Ala)	rs140463385	0.00447
NM_022124.6(CDH23):c.10026C>T (p.Asp3342=)	rs377118941	0.00185

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