ClinVar Miner

Submissions for variant NM_025081.3(NYNRIN):c.5493G>C (p.Gln1831His)

dbSNP: rs2139356308
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Oncology - Human Genetics Lab, University of Sao Paulo RCV001843907 SCV002103132 uncertain significance Hepatoblastoma no assertion criteria provided research

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