ClinVar Miner

Submissions for variant NM_003467.3(CXCR4):c.87C>T (p.Phe29=)

gnomAD frequency: 0.00004  dbSNP: rs768296315
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001422341 SCV001624884 likely benign Warts, hypogammaglobulinemia, infections, and myelokathexis 2023-07-28 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702593 SCV001930642 likely benign not provided no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001702593 SCV001963405 likely benign not provided no assertion criteria provided clinical testing

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