ClinVar Miner

Submissions for variant NM_152743.4(BRAT1):c.282+141A>C

gnomAD frequency: 0.02107  dbSNP: rs12666641
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001568769 SCV001792695 likely benign not provided 2018-07-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001568769 SCV005228343 likely benign not provided criteria provided, single submitter not provided

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