ClinVar Miner

Submissions for variant NM_147686.4(TRAF3IP2):c.454A>T (p.Thr152Ser)

gnomAD frequency: 0.00001  dbSNP: rs1796521013
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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 RCV001960097 SCV002211187 uncertain significance Candidiasis, familial, 8 2021-08-26 criteria provided, single submitter clinical testing

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