ClinVar Miner

Submissions for variant NM_001360016.2(G6PD):c.1195del (p.Ala399fs)

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Total submissions: 1
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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 RCV004764600 SCV005374143 pathogenic Anemia, nonspherocytic hemolytic, due to G6PD deficiency 2024-09-22 criteria provided, single submitter clinical testing

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