ClinVar Miner

Submissions for variant NM_144585.4(SLC22A12):c.-220G>A

gnomAD frequency: 0.50493  dbSNP: rs3825018
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000275434 SCV000372966 benign Dalmatian hypouricemia 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001672453 SCV001883873 benign not provided 2018-11-12 criteria provided, single submitter clinical testing

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