ClinVar Miner

Submissions for variant NM_004260.3(RECQL4):c.1704+9C>T (rs35876881)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000173798 SCV000224950 likely benign not specified 2015-06-09 criteria provided, single submitter clinical testing
Invitae RCV000988131 SCV000288188 benign Baller-Gerold syndrome 2019-12-31 criteria provided, single submitter clinical testing
Mendelics RCV000988131 SCV001137729 likely benign Baller-Gerold syndrome 2019-05-28 criteria provided, single submitter clinical testing

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