ClinVar Miner

Submissions for variant NM_000233.4(LHCGR):c.1505T>C (p.Leu502Pro) (rs121912538)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000015491 SCV000035756 pathogenic Leydig cell agenesis 2004-10-01 no assertion criteria provided literature only

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