ClinVar Miner

Submissions for variant NM_147686.4(TRAF3IP2):c.981C>T (p.Pro327=)

gnomAD frequency: 0.00004  dbSNP: rs112036127
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 RCV000910724 SCV001055611 likely benign Candidiasis, familial, 8 2024-01-18 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003424467 SCV004160001 likely benign not provided 2022-07-01 criteria provided, single submitter clinical testing TRAF3IP2: BP4, BP7

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