ClinVar Miner

Submissions for variant NM_174878.3(CLRN1):c.*277GT[15]

dbSNP: rs34027634
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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 RCV000316048 SCV000441690 uncertain significance Retinitis Pigmentosa, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000379991 SCV000441691 uncertain significance Retinitis pigmentosa-deafness syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001594979 SCV001828139 benign not provided 2019-08-26 criteria provided, single submitter clinical testing

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