ClinVar Miner

Submissions for variant NM_001127644.2(GABRA1):c.-15-9A>T

gnomAD frequency: 0.00001  dbSNP: rs770530140
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000827367 SCV000969010 likely benign not provided 2021-02-16 criteria provided, single submitter clinical testing

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