ClinVar Miner

Submissions for variant NM_003467.3(CXCR4):c.528C>T (p.Asn176=)

gnomAD frequency: 0.00001  dbSNP: rs113338664
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001404670 SCV001606577 likely benign Warts, hypogammaglobulinemia, infections, and myelokathexis 2022-10-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711426 SCV005262870 likely benign not provided criteria provided, single submitter not provided

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