ClinVar Miner

Submissions for variant NM_001370466.1(NOD2):c.32G>T (p.Arg11Met)

gnomAD frequency: 0.00004  dbSNP: rs104895487
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Unité médicale des maladies autoinflammatoires, CHRU Montpellier RCV000084075 SCV000116203 not provided Blau syndrome no assertion provided not provided

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