ClinVar Miner

Submissions for variant NM_001379180.1(ESRRB):c.1120+9G>A

gnomAD frequency: 0.00024  dbSNP: rs377532399
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 RCV002099860 SCV002324917 likely benign not provided 2024-10-26 criteria provided, single submitter clinical testing

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