ClinVar Miner

Submissions for variant NM_001360016.2(G6PD):c.686A>T (p.Asn229Ile)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003120160 SCV003799844 uncertain significance not provided 2022-03-30 criteria provided, single submitter clinical testing

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