ClinVar Miner

Submissions for variant NM_006343.3(MERTK):c.1296+28T>G

gnomAD frequency: 0.23549  dbSNP: rs57297275
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001775520 SCV002014186 benign Retinitis pigmentosa 38 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004709137 SCV005239507 benign not provided criteria provided, single submitter not provided

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