ClinVar Miner

Submissions for variant NM_000233.3(LHCGR):c.1360G>A (p.Val454Ile) (rs114320052)

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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 RCV000731559 SCV000859397 uncertain significance not provided 2018-02-09 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000263657 SCV000431032 likely benign Hypergonadotropic hypogonadism 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000318790 SCV000431033 likely benign Gonadotropin-independent familial sexual precocity 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000373581 SCV000431034 likely benign Leydig cell agenesis 2016-06-14 criteria provided, single submitter clinical testing

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