ClinVar Miner

Submissions for variant NM_001039591.3(USP9X):c.5898A>T (p.Ile1966=)

gnomAD frequency: 0.00004  dbSNP: rs771783379
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 RCV000893413 SCV001037345 benign not provided 2024-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000893413 SCV001842997 benign not provided 2020-09-01 criteria provided, single submitter clinical testing

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