ClinVar Miner

Submissions for variant NM_001353921.2(ARHGEF9):c.16G>A (p.Gly6Ser)

dbSNP: rs2056441301
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Strasbourg University Hospital RCV001249524 SCV001423514 uncertain significance Autism spectrum disorder 2019-12-01 no assertion criteria provided clinical testing

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