ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.1393-168A>G

gnomAD frequency: 0.11997  dbSNP: rs7565682
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 RCV001710071 SCV001937953 benign not provided 2018-07-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001710071 SCV005241247 benign not provided criteria provided, single submitter not provided

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