ClinVar Miner

Submissions for variant NM_176824.3(BBS7):c.934+31_934+34del

dbSNP: rs111713350
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
PreventionGenetics, part of Exact Sciences RCV000242224 SCV000316607 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001640585 SCV001855830 benign not provided 2021-06-18 criteria provided, single submitter clinical testing

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