ClinVar Miner

Submissions for variant NM_000637.5(GSR):c.307G>A (p.Val103Met)

gnomAD frequency: 0.00001  dbSNP: rs745404470
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV002227355 SCV002506235 uncertain significance Hemolytic anemia due to glutathione reductase deficiency 2022-02-02 criteria provided, single submitter clinical testing

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