ClinVar Miner

List of variants in gene SLC2A1 reported as uncertain significance for carbohydrate metabolism disease

Included ClinVar conditions (161):
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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP
NM_006516.2(SLC2A1):c.-225T>G rs886046343
NM_006516.2(SLC2A1):c.-272G>A rs886046344
NM_006516.2(SLC2A1):c.-368A>C rs528964239
NM_006516.2(SLC2A1):c.-384G>A rs886046345
NM_006516.2(SLC2A1):c.-388G>T rs544483207
NM_006516.2(SLC2A1):c.-424C>G rs867977523
NM_006516.2(SLC2A1):c.-483G>T rs886046346
NM_006516.2(SLC2A1):c.-510G>C rs886046347
NM_006516.3(SLC2A1):c.*1016A>G rs886046334
NM_006516.3(SLC2A1):c.*1081T>A rs886046333
NM_006516.3(SLC2A1):c.*1147G>C rs886046332
NM_006516.3(SLC2A1):c.*1149C>A rs779668330
NM_006516.3(SLC2A1):c.*1205C>T rs886046331
NM_006516.3(SLC2A1):c.*1246G>A rs886046330
NM_006516.3(SLC2A1):c.*1281A>G rs1057515458
NM_006516.3(SLC2A1):c.*1337A>C rs113441673
NM_006516.3(SLC2A1):c.*1337A>G rs113441673
NM_006516.3(SLC2A1):c.*1564C>T rs1057515570
NM_006516.3(SLC2A1):c.*1611T>C rs1057515457
NM_006516.3(SLC2A1):c.*322T>G rs886046340
NM_006516.3(SLC2A1):c.*514G>T rs886046339
NM_006516.3(SLC2A1):c.*560T>C rs545613558
NM_006516.3(SLC2A1):c.*587A>T rs748209315
NM_006516.3(SLC2A1):c.*597G>A rs886046338
NM_006516.3(SLC2A1):c.*651G>T rs886046337
NM_006516.3(SLC2A1):c.*750T>A rs886046336
NM_006516.3(SLC2A1):c.*784A>G rs886046335
NM_006516.3(SLC2A1):c.-192G>C rs886046342
NM_006516.3(SLC2A1):c.1007_1009del (p.Leu336del) rs587784389
NM_006516.3(SLC2A1):c.1016T>C (p.Ile339Thr) rs141619735
NM_006516.3(SLC2A1):c.1062G>A (p.Ala354=) rs748983257
NM_006516.3(SLC2A1):c.132C>T (p.Tyr44=) rs886046341
NM_006516.3(SLC2A1):c.1395C>T (p.Ser465=) rs75852730
NM_006516.3(SLC2A1):c.141A>T (p.Thr47=) rs150863093
NM_006516.3(SLC2A1):c.172C>T (p.Pro58Ser) rs765479065
NM_006516.3(SLC2A1):c.18+12G>T rs587781171
NM_006516.3(SLC2A1):c.188C>T (p.Thr63Met) rs200828053
NM_006516.3(SLC2A1):c.192C>G (p.Leu64=) rs762583668
NM_006516.3(SLC2A1):c.274C>A (p.Arg92=) rs202060209
NM_006516.3(SLC2A1):c.313G>A (p.Val105Met) rs577667739
NM_006516.3(SLC2A1):c.411A>G (p.Thr137=) rs753500924
NM_006516.3(SLC2A1):c.517-1G>C rs869312673
NM_006516.3(SLC2A1):c.543C>T (p.Gly181=) rs377674001
NM_006516.3(SLC2A1):c.679+4C>A rs139492241
NM_006516.3(SLC2A1):c.680-10G>T rs587784394
NM_006516.3(SLC2A1):c.75G>A (p.Gln25=) rs1557651193
NM_006516.3(SLC2A1):c.764A>C (p.Lys255Thr) rs5811
NM_006516.3(SLC2A1):c.777C>T (p.Ile259=) rs78388808
NM_006516.3(SLC2A1):c.972+7del rs531385270
NM_006516.4(SLC2A1):c.*1079T>G
NM_006516.4(SLC2A1):c.*107G>A
NM_006516.4(SLC2A1):c.*1321T>A
NM_006516.4(SLC2A1):c.*216C>T
NM_006516.4(SLC2A1):c.*368A>C
NM_006516.4(SLC2A1):c.*413G>A
NM_006516.4(SLC2A1):c.*609G>C
NM_006516.4(SLC2A1):c.*775A>G
NM_006516.4(SLC2A1):c.*92G>A
NM_006516.4(SLC2A1):c.-129G>T
NM_006516.4(SLC2A1):c.-194G>A
NM_006516.4(SLC2A1):c.-202G>C
NM_006516.4(SLC2A1):c.218C>T (p.Ser73Phe)
NM_006516.4(SLC2A1):c.279G>A (p.Arg93=)
NM_006516.4(SLC2A1):c.332G>T (p.Gly111Val)
NM_006516.4(SLC2A1):c.601T>G (p.Cys201Gly) rs1050933017
NM_006516.4(SLC2A1):c.787T>C (p.Phe263Leu)

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