ClinVar Miner

Submissions for variant NM_004364.4(CEBPA):c.690G>T (p.Thr230=) (rs34529039)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000242634 SCV000310136 benign not specified criteria provided, single submitter clinical testing
GeneReviews RCV000020588 SCV000041075 benign Acute myeloid leukemia 2010-10-21 no assertion criteria provided curation Converted during submission to Benign.

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