ClinVar Miner

Submissions for variant NM_153447.4(NLRP5):c.622+253G>A

gnomAD frequency: 0.00006  dbSNP: rs199475767
Minimum review status: Collection method:
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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
Human Evolutionary Genetics, Institut Pasteur RCV000089557 SCV000122016 untested not provided no assertion provided not provided Converted during submission to not provided.

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