ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.4581G>A (p.Pro1527=) (rs78635099)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000242552 SCV000605206 benign not specified 2017-01-13 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000377534 SCV000396825 likely benign Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000377534 SCV000558661 benign Fanconi anemia 2017-12-21 criteria provided, single submitter clinical testing
PreventionGenetics RCV000242552 SCV000314944 benign not specified criteria provided, single submitter clinical testing

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