ClinVar Miner

Submissions for variant NM_000035.4(ALDOB):c.*612A>G (rs41296049)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000358465 SCV000476046 likely benign Hereditary fructosuria 2016-06-14 criteria provided, single submitter clinical testing

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