ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.3365C>T (p.Pro1122Leu) (rs714181)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000245084 SCV000314933 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000323962 SCV000396844 benign Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000245084 SCV000605195 benign not specified 2016-10-19 criteria provided, single submitter clinical testing
IntelligeneCG RCV000515613 SCV000611722 benign Fanconi anemia, complementation group P 2017-08-18 criteria provided, single submitter clinical testing
Invitae RCV000860480 SCV001000540 benign not provided 2019-03-05 criteria provided, single submitter clinical testing

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