ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.9331-99_9331-98dup

dbSNP: rs68156520
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
GeneDx RCV001568639 SCV001792546 likely benign not provided 2019-11-08 criteria provided, single submitter clinical testing
Natera, Inc. RCV001827494 SCV002082708 benign Cohen syndrome 2019-09-27 no assertion criteria provided clinical testing

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