ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.753G>A (p.Ala251=) (rs8061528)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000248107 SCV000314951 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000285095 SCV000396889 benign Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000248107 SCV000605194 benign not specified 2016-09-13 criteria provided, single submitter clinical testing

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