ClinVar Miner

Submissions for variant NM_001006657.2(WDR35):c.2599G>T (p.Val867Phe) (rs149667250)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000079360 SCV000111230 benign not specified 2013-10-10 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000375441 SCV000425999 likely benign Short Rib Polydactyly Syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000279775 SCV000426000 likely benign Cranioectodermal dysplasia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000545999 SCV000660379 benign not provided 2019-02-28 criteria provided, single submitter clinical testing

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