ClinVar Miner

Submissions for variant NM_138477.4(CDAN1):c.2937C>T (p.Ala979=)

gnomAD frequency: 0.00001  dbSNP: rs781767396
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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 RCV001802705 SCV002049760 likely benign Anemia, congenital dyserythropoietic, type 1a 2021-04-29 criteria provided, single submitter clinical testing
Invitae RCV003772216 SCV004636332 likely benign not provided 2022-12-15 criteria provided, single submitter clinical testing

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