ClinVar Miner

Submissions for variant NM_000949.7(PRLR):c.851T>G (p.Leu284Trp)

dbSNP: rs748942718
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medical Cytogenetics and Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano RCV001270198 SCV001364329 likely pathogenic Premature ovarian failure 2020-03-02 criteria provided, single submitter research

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