Variants in gene combination CDH23, PSAP with conflicting interpretations reported as "likely benign and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 14

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.*349A>G	rs1867978	0.77194
NM_002778.4(PSAP):c.1351-14A>G	rs4747203	0.34512
NM_002778.4(PSAP):c.*891G>A	rs7869	0.34207
NM_002778.4(PSAP):c.1350+5G>A	rs11000016	0.16762
NM_022124.6(CDH23):c.*204A>G	rs2290022	0.13799
NM_022124.6(CDH23):c.9319+11G>A	rs11000013	0.10868
NM_022124.6(CDH23):c.9873G>A (p.Thr3291=)	rs2290021	0.08719
NM_022124.6(CDH23):c.*510G>A	rs1054635	0.07812
NM_022124.6(CDH23):c.9373T>C (p.Phe3125Leu)	rs45583140	0.04021
NM_022124.6(CDH23):c.9758A>C (p.Asp3253Ala)	rs140463385	0.00447
NM_022124.6(CDH23):c.9510+13C>T	rs183692794	0.00379
NM_022124.6(CDH23):c.9903C>T (p.Pro3301=)	rs55717455	0.00341
NM_022124.6(CDH23):c.9501G>A (p.Thr3167=)	rs144906721	0.00292
NM_022124.6(CDH23):c.10026C>T (p.Asp3342=)	rs377118941	0.00185

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