ClinVar Miner

Submissions for variant NM_014290.3(TDRD7):c.207+19G>A

gnomAD frequency: 0.00568  dbSNP: rs16920147
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000253542 SCV000312125 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001541161 SCV001759123 benign not provided 2021-01-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058246 SCV002405133 benign Cataract 36 2024-01-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001541161 SCV005265108 benign not provided criteria provided, single submitter not provided

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