ClinVar Miner

Submissions for variant NM_021252.5(RAB18):c.260-43_260-42del

dbSNP: rs72201756
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001611049 SCV001836735 benign not provided 2018-10-17 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001796607 SCV002033383 benign Warburg micro syndrome 3 2021-11-07 criteria provided, single submitter clinical testing

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