ClinVar Miner

Submissions for variant NM_006420.3(ARFGEF2):c.4755+19A>G

gnomAD frequency: 0.36848  dbSNP: rs7270848
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252371 SCV000311492 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001610672 SCV001836430 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Invitae RCV001610672 SCV002487152 benign not provided 2024-02-01 criteria provided, single submitter clinical testing

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