ClinVar Miner

Submissions for variant NM_001029883.3(PCARE):c.3673_3675dupAGC

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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000382560 SCV000341214 benign not specified 2016-04-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000278051 SCV000429853 likely benign Retinitis Pigmentosa, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Mendelics RCV000986607 SCV001135644 benign Retinitis pigmentosa 54 2019-05-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001511102 SCV001718290 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Dept Of Ophthalmology, Nagoya University RCV003888792 SCV004705293 benign Retinal dystrophy 2023-10-01 criteria provided, single submitter research
Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg RCV004816574 SCV005070765 uncertain significance Optic atrophy 2023-01-01 no assertion criteria provided clinical testing
Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg RCV003888792 SCV005073490 uncertain significance Retinal dystrophy 2023-01-01 no assertion criteria provided clinical testing

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