ClinVar Miner

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

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_020041.3(SLC2A9):c.1046C>T (p.Pro349Leu) rs116742917
NM_020041.3(SLC2A9):c.1049C>T (p.Pro350Leu) rs2280205
NM_020041.3(SLC2A9):c.1113+9A>C rs2280204
NM_020041.3(SLC2A9):c.322T>C (p.Leu108=) rs13113918
NM_020041.3(SLC2A9):c.375G>A (p.Thr125=) rs10939650
NM_020041.3(SLC2A9):c.504C>T (p.Ile168=) rs3733589
NM_020041.3(SLC2A9):c.567T>C (p.Leu189=) rs13125646
NM_020041.3(SLC2A9):c.73G>A (p.Gly25Arg) rs2276961
NM_020041.3(SLC2A9):c.841G>C (p.Asp281His) rs73225891
NM_020041.3(SLC2A9):c.844G>A (p.Val282Ile) rs16890979
NM_020041.3(SLC2A9):c.881G>A (p.Arg294His) rs3733591

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