ClinVar Miner

Submissions for variant NM_003041.4(SLC5A2):c.416G>A (p.Arg139His)

dbSNP: rs1378076282
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000625874 SCV000746449 uncertain significance Familial renal glucosuria 2020-05-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV000625874 SCV002788537 uncertain significance Familial renal glucosuria 2022-01-03 criteria provided, single submitter clinical testing

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