ClinVar Miner

List of variants in gene SLC2A2 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: 35
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HGVS dbSNP
NM_000340.1(SLC2A2):c.-238A>G rs551728717
NM_000340.2(SLC2A2):c.*1086G>A rs185726034
NM_000340.2(SLC2A2):c.*1164T>C rs886058171
NM_000340.2(SLC2A2):c.*11C>G rs761913998
NM_000340.2(SLC2A2):c.*1260A>G rs573454591
NM_000340.2(SLC2A2):c.*153A>G rs530625053
NM_000340.2(SLC2A2):c.*325del rs886058174
NM_000340.2(SLC2A2):c.*486T>C rs566222124
NM_000340.2(SLC2A2):c.*568A>T rs886058173
NM_000340.2(SLC2A2):c.*607del rs563605045
NM_000340.2(SLC2A2):c.*726T>C rs886058172
NM_000340.2(SLC2A2):c.*796T>C rs140738490
NM_000340.2(SLC2A2):c.*7_*8dup (p.Ter525=) rs573575421
NM_000340.2(SLC2A2):c.*8del (p.Ter525=) rs573575421
NM_000340.2(SLC2A2):c.*94del rs886058175
NM_000340.2(SLC2A2):c.-48G>A rs372965718
NM_000340.2(SLC2A2):c.1039G>A (p.Ala347Thr) rs776435170
NM_000340.2(SLC2A2):c.1069-10A>G rs1487335649
NM_000340.2(SLC2A2):c.112_114ATA[1] (p.Ile39del) rs772999215
NM_000340.2(SLC2A2):c.1169T>G (p.Leu390Arg) rs760200790
NM_000340.2(SLC2A2):c.1221T>C (p.Phe407=) rs775605288
NM_000340.2(SLC2A2):c.1295G>A (p.Arg432His) rs75144723
NM_000340.2(SLC2A2):c.1402C>G (p.Leu468Val) rs140138702
NM_000340.2(SLC2A2):c.1432C>G (p.Leu478Val) rs5397
NM_000340.2(SLC2A2):c.1489_1490delinsAA (p.Ala497Lys) rs1560031152
NM_000340.2(SLC2A2):c.15+6G>A rs886058177
NM_000340.2(SLC2A2):c.158G>A (p.Arg53Gln) rs145210664
NM_000340.2(SLC2A2):c.206C>A (p.Thr69Lys) rs779977931
NM_000340.2(SLC2A2):c.247G>A (p.Glu83Lys) rs150851401
NM_000340.2(SLC2A2):c.379G>T (p.Ala127Ser)
NM_000340.2(SLC2A2):c.580C>G (p.Leu194Val) rs779065938
NM_000340.2(SLC2A2):c.593C>T (p.Thr198Met) rs149460434
NM_000340.2(SLC2A2):c.612+10C>A rs762632420
NM_000340.2(SLC2A2):c.639C>T (p.Gly213=) rs886058176
NM_000340.2(SLC2A2):c.797_799ATG[2] (p.Asp268del) rs774721090

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