ClinVar Miner

Submissions for variant NM_177987.3(TUBB8):c.516G>A (p.Ser172=)

dbSNP: rs9329305
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001543795 SCV001762658 benign Oocyte maturation defect 2 2021-07-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004718889 SCV005320416 benign not provided criteria provided, single submitter not provided

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