ClinVar Miner

Submissions for variant NM_020754.4(ARHGAP31):c.1926+89T>A

gnomAD frequency: 0.38289  dbSNP: rs12636976
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001698819 SCV001916701 benign not provided 2019-04-20 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260357 SCV002539435 benign Adams-Oliver syndrome 1 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001698819 SCV005302941 benign not provided criteria provided, single submitter not provided

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