ClinVar Miner

Submissions for variant NM_000554.6(CRX):c.*1900del

dbSNP: rs796977583
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000328909 SCV000414096 benign Cone-Rod Dystrophy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000385852 SCV000414097 benign Leber congenital amaurosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000293870 SCV000414098 benign Retinitis Pigmentosa, Dominant 2016-06-14 criteria provided, single submitter clinical testing

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