ClinVar Miner

Submissions for variant NM_000233.4(LHCGR):c.*281del

dbSNP: rs558291070
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000371037 SCV000431005 likely benign Leydig cell agenesis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000408420 SCV000431006 likely benign Hypergonadotropic hypogonadism 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000312867 SCV000431007 likely benign Gonadotropin-independent familial sexual precocity 2016-06-14 criteria provided, single submitter clinical testing

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