ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.9331-3dup

dbSNP: rs370235149
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV001355938 SCV005196063 uncertain significance not provided criteria provided, single submitter not provided
Department of Pathology and Laboratory Medicine, Sinai Health System RCV001355938 SCV001550968 uncertain significance not provided no assertion criteria provided clinical testing

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