ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.1393-167A>C

gnomAD frequency: 0.11996  dbSNP: rs7565683
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 RCV001616550 SCV001840302 benign not provided 2018-07-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001616550 SCV005241248 benign not provided criteria provided, single submitter not provided

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