ClinVar Miner

Submissions for variant NM_006420.3(ARFGEF2):c.4455-1G>A

dbSNP: rs2091537662
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
Department of Molecular Bıology and Genetics, Istanbul Technical University RCV001290449 SCV001427057 likely pathogenic Periventricular laminar heterotopia no assertion criteria provided research

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