ClinVar Miner

Submissions for variant NM_144773.4(PROKR2):c.208G>T (p.Gly70Cys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005029108 SCV005660842 uncertain significance Hypogonadotropic hypogonadism 3 with or without anosmia 2024-04-25 criteria provided, single submitter clinical testing

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