ClinVar Miner

Submissions for variant NM_019098.5(CNGB3):c.74G>A (p.Arg25His)

dbSNP: rs141098074
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001213369 SCV001384997 likely benign not provided 2024-01-04 criteria provided, single submitter clinical testing
Natera, Inc. RCV001828702 SCV002078493 uncertain significance Achromatopsia 2020-03-24 no assertion criteria provided clinical testing

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