ClinVar Miner

List of variants in gene SLC2A9 reported as uncertain significance 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: 15
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HGVS dbSNP
NM_020041.3(SLC2A9):c.*48C>G rs886059751
NM_020041.3(SLC2A9):c.1085G>A (p.Gly362Asp) rs367692082
NM_020041.3(SLC2A9):c.1124T>C (p.Ile375Thr) rs755325843
NM_020041.3(SLC2A9):c.1138C>T (p.Arg380Trp) rs121908321
NM_020041.3(SLC2A9):c.1356C>T (p.Ile452=) rs762605826
NM_020041.3(SLC2A9):c.1368C>T (p.Thr456=) rs375423927
NM_020041.3(SLC2A9):c.1392T>C (p.Ala464=) rs886059752
NM_020041.3(SLC2A9):c.1399C>A (p.Leu467Ile) rs779780913
NM_020041.3(SLC2A9):c.1413C>A (p.Phe471Leu) rs745845092
NM_020041.3(SLC2A9):c.250-9T>C rs770788275
NM_020041.3(SLC2A9):c.354dup (p.Ile119fs) rs772429581
NM_020041.3(SLC2A9):c.512G>A (p.Arg171His) rs769968441
NM_020041.3(SLC2A9):c.843C>T (p.Asp281=) rs374095603
NM_020041.3(SLC2A9):c.879C>G (p.Ser293Arg) rs886059753
NM_020041.3(SLC2A9):c.957C>T (p.Thr319=) rs770758004

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