ClinVar Miner

Submissions for variant NM_003467.3(CXCR4):c.153T>A (p.Thr51=)

gnomAD frequency: 0.00021  dbSNP: rs145879963
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000415760 SCV000493355 uncertain significance not provided 2016-08-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001437685 SCV001640545 likely benign Warts, hypogammaglobulinemia, infections, and myelokathexis 2023-08-27 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000415760 SCV001715724 uncertain significance not provided 2020-07-24 criteria provided, single submitter clinical testing

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