ClinVar Miner

Submissions for variant NM_016734.3(PAX5):c.1110C>T (p.Tyr370=)

gnomAD frequency: 0.76812  dbSNP: rs3780135
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001657766 SCV001872198 benign not provided 2019-01-10 criteria provided, single submitter clinical testing
Invitae RCV001657766 SCV003201893 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
ITMI RCV000121765 SCV000085963 not provided not specified 2013-09-19 no assertion provided reference population

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