ClinVar Miner

List of variants in gene GLIS2 studied 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: 78
Download table as spreadsheet
HGVS dbSNP
GLIS2, IVS5DS, G-T, +1
NC_000016.9:g.(?_4386706)_(4387545_?)dup
NM_001318918.1(GLIS2):c.*1046G>C rs886051998
NM_001318918.1(GLIS2):c.*1082G>A rs886051999
NM_001318918.1(GLIS2):c.*1130G>A rs7197512
NM_001318918.1(GLIS2):c.*1161G>A rs78428657
NM_001318918.1(GLIS2):c.*1176C>T rs150762287
NM_001318918.1(GLIS2):c.*1203C>G rs116981725
NM_001318918.1(GLIS2):c.*12G>A rs201860422
NM_001318918.1(GLIS2):c.*1333C>G rs11544635
NM_001318918.1(GLIS2):c.*1465G>A rs762692214
NM_001318918.1(GLIS2):c.*1583del rs886052000
NM_001318918.1(GLIS2):c.*1628C>G rs886052001
NM_001318918.1(GLIS2):c.*1700G>A rs886052002
NM_001318918.1(GLIS2):c.*173G>A rs139029261
NM_001318918.1(GLIS2):c.*1761C>T rs370625022
NM_001318918.1(GLIS2):c.*1791T>C rs886052003
NM_001318918.1(GLIS2):c.*1826C>T rs757541
NM_001318918.1(GLIS2):c.*1830C>T rs578236633
NM_001318918.1(GLIS2):c.*1988A>G rs139152543
NM_001318918.1(GLIS2):c.*232T>G rs114705511
NM_001318918.1(GLIS2):c.*23G>A rs146555568
NM_001318918.1(GLIS2):c.*278C>T rs116692282
NM_001318918.1(GLIS2):c.*291_*293TCC[1] rs377612419
NM_001318918.1(GLIS2):c.*2C>T rs144489623
NM_001318918.1(GLIS2):c.*399T>G rs189481658
NM_001318918.1(GLIS2):c.*437A>C rs533863589
NM_001318918.1(GLIS2):c.*43G>A rs184772323
NM_001318918.1(GLIS2):c.*525C>T rs886051991
NM_001318918.1(GLIS2):c.*54C>T rs368483996
NM_001318918.1(GLIS2):c.*551C>G rs886051992
NM_001318918.1(GLIS2):c.*611G>A rs886051993
NM_001318918.1(GLIS2):c.*614G>A rs653539
NM_001318918.1(GLIS2):c.*632G>A rs886051994
NM_001318918.1(GLIS2):c.*712C>G rs886051995
NM_001318918.1(GLIS2):c.*762C>T rs573926229
NM_001318918.1(GLIS2):c.*796G>C rs111818339
NM_001318918.1(GLIS2):c.*856C>T rs886051996
NM_001318918.1(GLIS2):c.*881C>T rs540618522
NM_001318918.1(GLIS2):c.*887G>C rs886051997
NM_001318918.1(GLIS2):c.*916G>A rs72766567
NM_001318918.1(GLIS2):c.-11G>A rs28449480
NM_001318918.1(GLIS2):c.1010C>T (p.Pro337Leu) rs140544340
NM_001318918.1(GLIS2):c.1011G>A (p.Pro337=) rs200814551
NM_001318918.1(GLIS2):c.101G>A (p.Arg34His) rs377037409
NM_001318918.1(GLIS2):c.1105G>A (p.Gly369Ser) rs200720013
NM_001318918.1(GLIS2):c.1128C>T (p.Pro376=) rs750906253
NM_001318918.1(GLIS2):c.1180G>A (p.Gly394Ser) rs775114398
NM_001318918.1(GLIS2):c.1194_1208dup (p.Gly401_Pro405dup) rs878855164
NM_001318918.1(GLIS2):c.1259C>T (p.Pro420Leu) rs75495782
NM_001318918.1(GLIS2):c.1273G>A (p.Gly425Arg) rs199849300
NM_001318918.1(GLIS2):c.127G>A (p.Val43Met) rs886051989
NM_001318918.1(GLIS2):c.1311A>C (p.Ala437=) rs3810817
NM_001318918.1(GLIS2):c.1326C>T (p.Ala442=) rs767819594
NM_001318918.1(GLIS2):c.1335G>C (p.Glu445Asp) rs761985295
NM_001318918.1(GLIS2):c.1350G>A (p.Ser450=) rs150464446
NM_001318918.1(GLIS2):c.1355C>A (p.Pro452His) rs776535774
NM_001318918.1(GLIS2):c.1388C>T (p.Thr463Met)
NM_001318918.1(GLIS2):c.1403C>T (p.Thr468Met) rs138285254
NM_001318918.1(GLIS2):c.1413C>G (p.Ser471Arg) rs201182025
NM_001318918.1(GLIS2):c.1431C>T (p.Pro477=) rs150810544
NM_001318918.1(GLIS2):c.1474A>G (p.Thr492Ala) rs8057701
NM_001318918.1(GLIS2):c.1476G>A (p.Thr492=) rs140403969
NM_001318918.1(GLIS2):c.1539G>A (p.Pro513=) rs769088578
NM_001318918.1(GLIS2):c.1569G>A (p.Val523=) rs371022001
NM_001318918.1(GLIS2):c.18G>A (p.Glu6=) rs759679058
NM_001318918.1(GLIS2):c.210G>A (p.Glu70=) rs886051990
NM_001318918.1(GLIS2):c.223G>T (p.Ala75Ser) rs72766563
NM_001318918.1(GLIS2):c.291G>A (p.Ser97=) rs529581775
NM_001318918.1(GLIS2):c.344C>T (p.Ser115Leu) rs771450245
NM_001318918.1(GLIS2):c.505G>A (p.Val169Met) rs144844035
NM_001318918.1(GLIS2):c.523T>C (p.Cys175Arg) rs587777353
NM_001318918.1(GLIS2):c.651C>T (p.Asn217=) rs140609747
NM_001318918.1(GLIS2):c.693C>T (p.Asn231=) rs150071733
NM_001318918.1(GLIS2):c.747C>T (p.Asn249=) rs763296256
NM_001318918.1(GLIS2):c.775+1G>T rs878855335
NM_001318918.1(GLIS2):c.864T>C (p.Tyr288=) rs669561
NM_001318918.1(GLIS2):c.894C>T (p.Pro298=) rs112926217

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.