ClinVar Miner

Submissions for variant NM_198053.3(CD247):c.100C>T (p.Leu34=)

gnomAD frequency: 0.00017  dbSNP: rs181342622
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000897557 SCV001041708 benign Immunodeficiency 25 2024-01-06 criteria provided, single submitter clinical testing

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