ClinVar Miner

Submissions for variant NM_002894.3(RBBP8):c.807+182A>G

gnomAD frequency: 0.05132  dbSNP: rs78074885
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001725600 SCV001960591 benign not provided 2018-08-17 criteria provided, single submitter clinical testing

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