ClinVar Miner

Submissions for variant NM_031296.2(RAB33B):c.-205G>C

gnomAD frequency: 0.20381  dbSNP: rs13126617
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000315111 SCV000447486 benign Smith-McCort dysplasia 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001672637 SCV001888920 benign not provided 2018-11-12 criteria provided, single submitter clinical testing

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