ClinVar Miner

Submissions for variant NM_000402.4(G6PD):c.1172C>T (p.Ala391Val) (rs137852345)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000011153 SCV000031380 other G6PD SERRES 2017-05-24 no assertion criteria provided literature only
OMIM RCV000143788 SCV000188682 pathogenic Anemia, nonspherocytic hemolytic, due to G6PD deficiency 2017-05-24 no assertion criteria provided literature only

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