ClinVar Miner

Submissions for variant NM_001127671.2(LIFR):c.143-37GT[15] (rs10637374)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000177150 SCV000228981 benign not specified 2015-01-17 criteria provided, single submitter clinical testing
Invitae RCV001522166 SCV001731650 benign not provided 2020-11-25 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV000177150 SCV001808856 benign not specified no assertion criteria provided clinical testing

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