ClinVar Miner

Submissions for variant NM_001291415.2(KDM6A):c.2333C>A (p.Thr778Lys) (rs2230018)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory,University of Chicago RCV000121287 SCV000193342 benign not specified 2013-08-01 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000121287 SCV000202892 benign not specified 2015-09-29 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000121287 SCV000313748 benign not specified criteria provided, single submitter clinical testing
ITMI RCV000121287 SCV000085458 not provided not specified 2013-09-19 no assertion provided reference population

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