ClinVar Miner

Submissions for variant NM_004744.5(LRAT):c.*2477_*2479del

dbSNP: rs769393659
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000379995 SCV000447980 uncertain significance Retinal dystrophy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000283200 SCV000447981 uncertain significance Retinitis Pigmentosa, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000340580 SCV000447982 uncertain significance Leber congenital amaurosis 2016-06-14 criteria provided, single submitter clinical testing

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