ClinVar Miner

Submissions for variant NM_006118.3(HAX1):c.207A>T (p.Pro69=) (rs142150013)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000502834 SCV000595091 likely benign not specified 2017-05-26 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000377509 SCV000348479 uncertain significance Severe congenital neutropenia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000532229 SCV000657555 benign Severe congenital neutropenia 3, autosomal recessive 2017-11-27 criteria provided, single submitter clinical testing

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