ClinVar Miner

Submissions for variant NM_006261.4(PROP1):c.152G>C (p.Gly51Ala) (rs2233783)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000417659 SCV000511491 benign not provided 2016-10-13 criteria provided, single submitter clinical testing
Counsyl RCV000169158 SCV000220385 benign Pituitary hormone deficiency, combined 2 2014-06-05 criteria provided, single submitter literature only
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000327755 SCV000341107 benign not specified 2016-04-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000382482 SCV000456759 likely benign Combined Pituitary Hormone Deficiency, Recessive 2016-06-14 criteria provided, single submitter clinical testing

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