ClinVar Miner

Submissions for variant NM_153447.4(NLRP5):c.2616-24G>A

gnomAD frequency: 0.00394  dbSNP: rs199475781
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Human Evolutionary Genetics, Institut Pasteur RCV000089546 SCV000122005 untested not provided no assertion provided not provided Converted during submission to not provided.

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