ClinVar Miner

Submissions for variant NM_147686.4(TRAF3IP2):c.1583A>G (p.His528Arg)

gnomAD frequency: 0.00044  dbSNP: rs202090066
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 RCV000887808 SCV001031394 benign Candidiasis, familial, 8 2024-01-24 criteria provided, single submitter clinical testing

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