ClinVar Miner

Submissions for variant NM_147686.4(TRAF3IP2):c.8G>A (p.Arg3Gln)

gnomAD frequency: 0.00015  dbSNP: rs148778036
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001405514 SCV001607441 likely benign Candidiasis, familial, 8 2023-12-03 criteria provided, single submitter clinical testing

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