Variants in gene CNGA3 with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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_001298.3(CNGA3):c.1279C>T (p.Arg427Cys)	rs141386891	0.00040
NM_001298.3(CNGA3):c.967G>C (p.Ala323Pro)	rs146195955	0.00030
NM_001298.3(CNGA3):c.811C>G (p.Pro271Ala)	rs149802213	0.00022
NM_001298.3(CNGA3):c.101+1G>A	rs147118493	0.00014
NM_001298.3(CNGA3):c.1669G>A (p.Gly557Arg)	rs104893615	0.00012
NM_001298.3(CNGA3):c.1034A>G (p.His345Arg)	rs780411290	0.00011
NM_001298.3(CNGA3):c.1982G>A (p.Arg661His)	rs144715956	0.00006
NM_001298.3(CNGA3):c.1557G>A (p.Met519Ile)	rs199655686	0.00004
NM_001298.3(CNGA3):c.1687C>T (p.Arg563Cys)	rs150153987	0.00003
NM_001298.3(CNGA3):c.1065T>G (p.Ser355Arg)	rs1277409725	0.00001
NM_001298.3(CNGA3):c.-37-1G>C	rs1553447991
NM_001298.3(CNGA3):c.1597G>C (p.Asp533His)	rs775332304
NM_001298.3(CNGA3):c.1609del (p.Gln537fs)	rs1293852552
NM_001298.3(CNGA3):c.1712T>C (p.Ile571Thr)	rs750456621

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