ClinVar Miner

Submissions for variant NM_005235.3(ERBB4):c.2706C>T (p.Asp902=)

gnomAD frequency: 0.00014  dbSNP: rs146441207
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000087212 SCV004284241 likely benign not provided 2023-11-17 criteria provided, single submitter clinical testing
Richard Lifton Laboratory, Yale University School of Medicine RCV000087212 SCV000120074 unknown not provided flagged submission not provided Converted during submission to Uncertain significance.
Richard Lifton Laboratory, Yale University School of Medicine RCV000087212 SCV000155178 unknown not provided no assertion criteria provided not provided Converted during submission to Uncertain significance.

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