ClinVar Miner

Submissions for variant NM_001360016.2(G6PD):c.1052-4G>A

gnomAD frequency: 0.00025  dbSNP: rs372124193
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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 RCV000967163 SCV001114534 likely benign Anemia, nonspherocytic hemolytic, due to G6PD deficiency 2024-12-10 criteria provided, single submitter clinical testing

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