ClinVar Miner

Submissions for variant NM_017950.4(CCDC40):c.1562+33G>A

gnomAD frequency: 0.06324  dbSNP: rs10083858
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
PreventionGenetics, part of Exact Sciences RCV000241962 SCV000313067 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001696199 SCV001916478 benign not provided 2018-07-10 criteria provided, single submitter clinical testing

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