ClinVar Miner

Submissions for variant NM_000342.4(SLC4A1):c.2508C>A (p.Phe836Leu)

dbSNP: rs2144596543
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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 RCV001811732 SCV002049515 uncertain significance not provided 2021-02-05 criteria provided, single submitter clinical testing

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