ClinVar Miner

Submissions for variant NM_020208.4(SLC6A20):c.-84G>T

gnomAD frequency: 0.00003  dbSNP: rs886058548
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000325307 SCV000444584 uncertain significance Hyperglycinuria 2016-06-14 criteria provided, single submitter clinical testing

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