Variants in gene CNGA3 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001298.3(CNGA3):c.740C>T (p.Thr247Met)	rs148616345	0.00158
NM_001298.3(CNGA3):c.198C>T (p.Thr66=)	rs139544302	0.00147
NM_001298.3(CNGA3):c.1618G>A (p.Val540Ile)	rs116448158	0.00113
NM_001298.3(CNGA3):c.284C>T (p.Pro95Leu)	rs114108462	0.00083
NM_001298.3(CNGA3):c.682G>A (p.Glu228Lys)	rs147415641	0.00049
NM_001298.3(CNGA3):c.473C>T (p.Ala158Val)	rs138934573	0.00022
NM_001298.3(CNGA3):c.1831C>T (p.Leu611=)	rs747855074	0.00001

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