ClinVar Miner

Submissions for variant NM_001059.3(TACR3):c.278G>A (p.Gly93Asp)

gnomAD frequency: 0.00001  dbSNP: rs121918124
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000030897 SCV000035325 pathogenic Hypogonadotropic hypogonadism 11 with or without anosmia 2009-03-01 no assertion criteria provided literature only
UniProtKB/Swiss-Prot RCV000059784 SCV000091354 not provided not provided no assertion provided not provided

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