ClinVar Miner

Submissions for variant NM_001127671.2(LIFR):c.143-37GT[11] (rs10637374)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000273147 SCV000457604 uncertain significance Stüve-Wiedemann syndrome 2016-06-14 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000727652 SCV000854956 benign not specified 2018-04-05 criteria provided, single submitter clinical testing
Invitae RCV000908352 SCV001053108 likely benign not provided 2020-12-06 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000273147 SCV001159605 benign Stüve-Wiedemann syndrome 2020-06-08 criteria provided, single submitter clinical testing

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