ClinVar Miner

Submissions for variant NM_001006657.2(WDR35):c.1058G>C (p.Arg353Pro) (rs76623454)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000337062 SCV000426044 uncertain significance Short Rib Polydactyly Syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000375359 SCV000426045 uncertain significance Cranioectodermal dysplasia 2016-06-14 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000507596 SCV000605606 benign not provided 2017-11-28 criteria provided, single submitter clinical testing

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