ClinVar Miner

Submissions for variant NM_001360016.2(G6PD):c.121-4460del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dunham Lab, University of Washington RCV002305839 SCV002599139 benign Anemia, nonspherocytic hemolytic, due to G6PD deficiency 2022-08-12 criteria provided, single submitter curation Variant found at a frequency of over 32% in gnomAD (BA1).

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