ClinVar Miner

Submissions for variant NM_018117.12(WDR11):c.1306A>G (p.Ile436Val)

gnomAD frequency: 0.00128  dbSNP: rs34602786
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia RCV000238652 SCV000297281 uncertain significance not specified 2015-11-24 criteria provided, single submitter clinical testing
Invitae RCV000872959 SCV001014870 benign not provided 2022-06-16 criteria provided, single submitter clinical testing

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