ClinVar Miner

Submissions for variant NM_006915.3(RP2):c.807A>G (p.Glu269=)

gnomAD frequency: 0.00003  dbSNP: rs148517937
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001472167 SCV001676295 likely benign not provided 2023-09-24 criteria provided, single submitter clinical testing
Dr. Peter K. Rogan Lab, Western University RCV005912843 SCV007018155 not provided Nonpapillary renal cell carcinoma no classification provided in vitro

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