ClinVar Miner

Submissions for variant NM_006420.3(ARFGEF2):c.907+292C>T

gnomAD frequency: 0.00904  dbSNP: rs62212425
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001592110 SCV001822369 likely benign not provided 2018-10-01 criteria provided, single submitter clinical testing

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