ClinVar Miner

Submissions for variant NM_001138.2(AGRP):c.199G>A (p.Ala67Thr)

gnomAD frequency: 0.02970  dbSNP: rs5030980
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV003992146 SCV004809747 benign Inherited obesity 2024-04-04 criteria provided, single submitter clinical testing
OMIM RCV000007753 SCV000027954 association Obesity, late-onset 2019-08-30 no assertion criteria provided literature only
OMIM RCV000007754 SCV000027955 pathogenic Leanness, inherited 2004-04-30 no assertion criteria provided literature only

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