ClinVar Miner

Submissions for variant NM_002872.5(RAC2):c.203G>A (p.Arg68Gln)

dbSNP: rs1927109339
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
UOSD Laboratory of Genetics & Genomics of Rare Diseases, Istituto Giannina Gaslini RCV001267784 SCV001424102 uncertain significance Neutrophil immunodeficiency syndrome 2020-05-21 no assertion criteria provided clinical testing

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