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
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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

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