ClinVar Miner

Submissions for variant NM_001034853.2(RPGR):c.310+10T>C

gnomAD frequency: 0.00015  dbSNP: rs373028441
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 RCV001514477 SCV001722327 benign Primary ciliary dyskinesia 2024-11-13 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV002464459 SCV002759504 likely benign not provided 2016-12-19 criteria provided, single submitter clinical testing

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