ClinVar Miner

Submissions for variant NM_016065.4(MRPS16):c.34T>C (p.Tyr12His)

gnomAD frequency: 0.04804  dbSNP: rs7905009
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
Invitae RCV000677073 SCV001728616 benign not provided 2024-01-25 criteria provided, single submitter clinical testing
GeneDx RCV000677073 SCV001913654 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000677073 SCV000802910 benign not provided 2016-02-29 no assertion criteria provided clinical testing

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