ClinVar Miner

Submissions for variant NM_005957.4(MTHFR):c.773C>G (p.Pro258Arg) (rs1553186124)

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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 RCV000508460 SCV000604293 uncertain significance not specified 2017-02-27 criteria provided, single submitter clinical testing

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