ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.2824+97G>C

dbSNP: rs7840337
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001532824 SCV001748563 benign Cohen syndrome 2021-07-01 criteria provided, single submitter clinical testing
GeneDx RCV001615249 SCV001840894 benign not provided 2018-07-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001615249 SCV005267271 benign not provided criteria provided, single submitter not provided

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