ClinVar Miner

Submissions for variant NM_001163809.2(WDR81):c.5118T>C (p.Leu1706=)

gnomAD frequency: 0.00139  dbSNP: rs138211651
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
CeGaT Center for Human Genetics Tuebingen RCV000585024 SCV000692886 uncertain significance not provided 2017-07-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000585024 SCV001116817 benign not provided 2018-08-16 criteria provided, single submitter clinical testing

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