ClinVar Miner

Submissions for variant NM_023067.4(FOXL2):c.1045C>G (p.Arg349Gly)

gnomAD frequency: 0.00013  dbSNP: rs201840174
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ITMI RCV000121136 SCV000085304 not provided not specified 2013-09-19 no assertion provided reference population
Center for Reproductive Medicine, Shandong Provincial Hospital Affiliated to Shandong University RCV001657762 SCV001877110 likely pathogenic Genetic non-acquired premature ovarian failure 2019-10-01 no assertion criteria provided research

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