ClinVar Miner

Submissions for variant NM_147686.4(TRAF3IP2):c.191A>C (p.His64Pro)

gnomAD frequency: 0.00175  dbSNP: rs149246847
Minimum review status: Collection method:
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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 RCV000946966 SCV001093129 benign Candidiasis, familial, 8 2024-01-26 criteria provided, single submitter clinical testing

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