ClinVar Miner

Submissions for variant NM_006118.4(HAX1):c.399A>G (p.Pro133=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002760218 SCV003017068 likely benign Kostmann syndrome 2022-03-26 criteria provided, single submitter clinical testing

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