ClinVar Miner

Submissions for variant NM_000233.3(LHCGR):c.-58G>T

gnomAD frequency: 0.18447  dbSNP: rs10176989
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000401707 SCV000431083 benign Gonadotropin-independent familial sexual precocity 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000295770 SCV000431084 benign Leydig cell agenesis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000348327 SCV000431085 benign Hypergonadotropic hypogonadism 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001711952 SCV001946085 benign not provided 2018-07-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001711952 SCV005243610 benign not provided criteria provided, single submitter not provided

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