ClinVar Miner

Submissions for variant NM_020208.4(SLC6A20):c.263-32A>G

gnomAD frequency: 0.55677  dbSNP: rs2252547
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001611555 SCV001836060 benign not provided 2021-05-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001810128 SCV002056664 benign Hyperglycinuria 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001611555 SCV005241658 benign not provided criteria provided, single submitter not provided

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