ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.905+62A>G

gnomAD frequency: 0.39496  dbSNP: rs5771109
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
GeneDx RCV001644190 SCV001857667 benign not provided 2018-07-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001644190 SCV005275908 benign not provided criteria provided, single submitter not provided

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