ClinVar Miner

Submissions for variant NM_001286535.2(RAD9B):c.661G>A (p.Gly221Arg)

dbSNP: rs763079713
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Finnell Lab, Baylor College of Medicine RCV000855674 SCV000998455 likely pathogenic Neural tube defect no assertion criteria provided case-control In vitro functional study described this variant affects RAD9B's protein function.

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