ClinVar Miner

Submissions for variant NM_001360016.2(G6PD):c.1491G>A (p.Lys497=)

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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 RCV003621935 SCV004388606 likely benign Anemia, nonspherocytic hemolytic, due to G6PD deficiency 2022-12-13 criteria provided, single submitter clinical testing

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