ClinVar Miner

Submissions for variant NM_153252.5(BRWD3):c.31+23dup

dbSNP: rs200402115
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
Genome-Nilou Lab RCV001553919 SCV001775022 benign Intellectual disability, X-linked 93 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001673197 SCV001891463 benign not provided 2019-08-20 criteria provided, single submitter clinical testing

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