ClinVar Miner

Submissions for variant NM_147686.4(TRAF3IP2):c.1275T>C (p.Asn425=)

gnomAD frequency: 0.00003  dbSNP: rs571096374
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 RCV003581740 SCV001023933 likely benign Candidiasis, familial, 8 2023-12-06 criteria provided, single submitter clinical testing

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