ClinVar Miner

Submissions for variant NM_001177693.2(ARHGEF28):c.267G>A (p.Val89=)

gnomAD frequency: 0.00840  dbSNP: rs17552682
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000243468 SCV000306401 benign not specified criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001579991 SCV005301635 benign not provided criteria provided, single submitter not provided
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579991 SCV001809292 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000243468 SCV001920010 benign not specified no assertion criteria provided clinical testing

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