ClinVar Miner

Submissions for variant NM_003041.4(SLC5A2):c.451A>C (p.Ile151Leu)

dbSNP: rs146552221
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV001280861 SCV002798289 uncertain significance Familial renal glucosuria 2023-12-28 criteria provided, single submitter clinical testing
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare RCV001280861 SCV001468206 uncertain significance Familial renal glucosuria 2020-01-15 no assertion criteria provided clinical testing

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