ClinVar Miner

Submissions for variant NM_000554.6(CRX):c.*1621_*1623dup

dbSNP: rs59559801
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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 RCV000291052 SCV000414081 uncertain significance Retinitis Pigmentosa, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000348287 SCV000414082 uncertain significance Cone-Rod Dystrophy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000396442 SCV000414083 uncertain significance Leber congenital amaurosis 2016-06-14 criteria provided, single submitter clinical testing

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