ClinVar Miner

Submissions for variant NM_000342.4(SLC4A1):c.1403T>G (p.Leu468Arg)

dbSNP: rs2144613014
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001812537 SCV002049090 uncertain significance not provided 2021-08-06 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001812537 SCV003821385 uncertain significance not provided 2021-10-15 criteria provided, single submitter clinical testing

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