ClinVar Miner

Submissions for variant NM_002310.5(LIFR):c.1899A>G (p.Ile633Met) (rs2303743)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000174730 SCV000604098 benign not specified 2016-10-24 criteria provided, single submitter clinical testing
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000443237 SCV000511794 benign not provided 2017-01-05 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000174730 SCV000226091 benign not specified 2015-01-06 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000265907 SCV000457590 likely benign Stuve-Wiedemann syndrome 2016-06-14 criteria provided, single submitter clinical testing

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