ClinVar Miner

Submissions for variant NM_001360016.2(G6PD):c.1293G>A (p.Val431=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002712106 SCV003010945 likely benign Anemia, nonspherocytic hemolytic, due to G6PD deficiency 2022-03-18 criteria provided, single submitter clinical testing

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