ClinVar Miner

List of variants in gene SLC2A9 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP
NM_020041.3(SLC2A9):c.*110G>T rs144294717
NM_020041.3(SLC2A9):c.*129C>A rs550035001
NM_020041.3(SLC2A9):c.1203G>A (p.Thr401=) rs191072192
NM_020041.3(SLC2A9):c.1221C>T (p.His407=) rs369754879
NM_020041.3(SLC2A9):c.1299C>T (p.Ile433=) rs147534794
NM_020041.3(SLC2A9):c.150+9G>A rs138627925
NM_020041.3(SLC2A9):c.1545C>T (p.Ser515=) rs144428359
NM_020041.3(SLC2A9):c.1599T>C (p.Asp533=) rs146590565
NM_020041.3(SLC2A9):c.198C>G (p.Gly66=) rs374679729
NM_020041.3(SLC2A9):c.247C>A (p.Pro83Thr) rs776421301
NM_020041.3(SLC2A9):c.249+11G>T rs377565288
NM_020041.3(SLC2A9):c.351C>T (p.Phe117=) rs148002726
NM_020041.3(SLC2A9):c.592C>T (p.Arg198Cys) rs121908322
NM_020041.3(SLC2A9):c.666C>T (p.Pro222=) rs139449249
NM_020041.3(SLC2A9):c.681+13C>T rs202000076
NM_020041.3(SLC2A9):c.72C>T (p.Ala24=) rs138916724
NM_020041.3(SLC2A9):c.798G>A (p.Glu266=) rs762538548
NM_020041.3(SLC2A9):c.809T>C (p.Val270Ala) rs116183067
NM_020041.3(SLC2A9):c.824C>T (p.Thr275Met) rs112404957
NM_020041.3(SLC2A9):c.883G>A (p.Val295Met) rs75088806
NM_020041.3(SLC2A9):c.898C>T (p.Arg300Cys) rs74651202
NM_020041.3(SLC2A9):c.899G>A (p.Arg300His) rs145688560

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.