ClinVar Miner

Submissions for variant NM_001322934.2(NFKB2):c.1212G>T (p.Gly404=)

gnomAD frequency: 0.00399  dbSNP: rs55847683
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000973895 SCV001121684 benign Immunodeficiency, common variable, 10 2024-01-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004718802 SCV005322327 benign not provided criteria provided, single submitter not provided

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