ClinVar Miner

Submissions for variant NM_003039.3(SLC2A5):c.808C>T (p.Arg270Trp)

gnomAD frequency: 0.00001  dbSNP: rs779760381
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medical Research Institute, Tokyo Medical and Dental University RCV000190149 SCV000221999 association Long QT syndrome no assertion criteria provided research

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