ClinVar Miner

Submissions for variant NM_198391.3(FLRT3):c.290A>G (p.Glu97Gly)

dbSNP: rs398124651
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000043602 SCV000071620 risk factor HYPOGONADOTROPIC HYPOGONADISM 21 WITH ANOSMIA, SUSCEPTIBILITY TO 2013-05-02 no assertion criteria provided literature only

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