ClinVar Miner

Submissions for variant NM_001367624.2(ZNF469):c.*618T>G

dbSNP: rs3859020
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000318656 SCV000399483 benign Brittle cornea syndrome 1 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004709541 SCV005249656 benign not provided criteria provided, single submitter not provided

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