ClinVar Miner

Submissions for variant NM_016734.3(PAX5):c.435G>C (p.Gln145His)

dbSNP: rs758368747
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000714779 SCV000845507 uncertain significance Acute lymphoid leukemia 2018-08-07 criteria provided, single submitter clinical testing

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