ClinVar Miner

Submissions for variant NM_006118.4(HAX1):c.678C>T (p.Arg226=)

dbSNP: rs1684911540
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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 RCV002107057 SCV002326456 likely benign Kostmann syndrome 2021-06-06 criteria provided, single submitter clinical testing

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