ClinVar Miner

Submissions for variant NM_007212.4(RNF2):c.902A>G (p.Gln301Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein RCV003991077 SCV004808396 uncertain significance Luo-Schoch-Yamamoto syndrome 2023-03-20 no assertion criteria provided clinical testing

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