ClinVar Miner

Submissions for variant NM_020923.3(ZDBF2):c.5795G>A (p.Arg1932His)

gnomAD frequency: 0.00006  dbSNP: rs763186071
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Next Generation Diagnostics, Novartis Institutes for BioMedical Research, Inc. RCV000207277 SCV000258646 uncertain significance Breast ductal adenocarcinoma 2015-07-20 no assertion criteria provided research

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