ClinVar Miner

Submissions for variant NM_198053.3(CD247):c.336+20C>T

gnomAD frequency: 0.00010  dbSNP: rs377122263
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 RCV001443537 SCV001646512 likely benign Immunodeficiency 25 2024-01-25 criteria provided, single submitter clinical testing

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