ClinVar Miner

Submissions for variant NM_000814.6(GABRB3):c.241-7715C>T

dbSNP: rs13329457
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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 RCV001615615 SCV001835734 benign not provided 2018-07-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001615615 SCV005297422 benign not provided criteria provided, single submitter not provided

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