ClinVar Miner

Submissions for variant NM_004663.5(RAB11A):c.237-20A>G

gnomAD frequency: 0.06152  dbSNP: rs74845010
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
GeneDx RCV001689012 SCV001911584 benign not provided 2018-10-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001689012 SCV002407087 benign not provided 2025-02-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001689012 SCV005292988 benign not provided criteria provided, single submitter not provided

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