ClinVar Miner

Submissions for variant NM_018206.6(VPS35):c.2222A>C (p.Gln741Pro)

dbSNP: rs547805228
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
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001795678 SCV002035230 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001795678 SCV002037861 uncertain significance not provided no assertion criteria provided clinical testing

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