ClinVar Miner

Submissions for variant NM_178857.6(RP1L1):c.2644C>T (p.Arg882Trp) (rs148936402)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000329036 SCV000471176 likely benign Occult macular dystrophy 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000762490 SCV000892815 uncertain significance not provided 2018-09-30 criteria provided, single submitter clinical testing

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