ClinVar Miner

Submissions for variant NM_004218.4(RAB11B):c.419G>A (p.Arg140His)

gnomAD frequency: 0.00002  dbSNP: rs374943563
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001936021 SCV002191914 likely benign not provided 2025-02-03 criteria provided, single submitter clinical testing

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