ClinVar Miner

Submissions for variant NM_177987.3(TUBB8):c.-51G>A

gnomAD frequency: 0.96261  dbSNP: rs6560830
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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 RCV001543800 SCV001762663 benign Oocyte maturation defect 2 2021-07-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004718894 SCV005321164 benign not provided criteria provided, single submitter not provided

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