ClinVar Miner

Submissions for variant NM_001177693.2(ARHGEF28):c.4161+16T>C

gnomAD frequency: 0.00742  dbSNP: rs200381893
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
Breakthrough Genomics, Breakthrough Genomics RCV001579824 SCV005223735 likely benign not provided criteria provided, single submitter not provided
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579824 SCV001808634 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001701204 SCV001922541 benign not specified no assertion criteria provided clinical testing

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