ClinVar Miner

Submissions for variant NM_006343.3(MERTK):c.61+19G>A

gnomAD frequency: 0.03962  dbSNP: rs115821982
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000301804 SCV000341270 benign not specified 2016-04-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001511846 SCV001719155 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001775756 SCV002014182 benign Retinitis pigmentosa 38 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001511846 SCV005239500 benign not provided criteria provided, single submitter not provided

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