ClinVar Miner

Submissions for variant NM_000554.6(CRX):c.*1122G>C (rs73576710)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000373918 SCV000414057 benign Leber congenital amaurosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000281627 SCV000414058 benign Retinitis Pigmentosa, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000338965 SCV000414059 benign Cone-Rod Dystrophy, Dominant 2016-06-14 criteria provided, single submitter clinical testing

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