ClinVar Miner

List of variants in gene GLIS2 studied 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: 83
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HGVS dbSNP
GLIS2, IVS5DS, G-T, +1
NC_000016.9:g.(?_4386706)_(4387545_?)dup
NM_032575.2(GLIS2):c.*1046G>C rs886051998
NM_032575.2(GLIS2):c.*1082G>A rs886051999
NM_032575.2(GLIS2):c.*1130G>A rs7197512
NM_032575.2(GLIS2):c.*1161G>A rs78428657
NM_032575.2(GLIS2):c.*1176C>T rs150762287
NM_032575.2(GLIS2):c.*1203C>G rs116981725
NM_032575.2(GLIS2):c.*12G>A rs201860422
NM_032575.2(GLIS2):c.*1333C>G rs11544635
NM_032575.2(GLIS2):c.*1465G>A rs762692214
NM_032575.2(GLIS2):c.*1583delC rs886052000
NM_032575.2(GLIS2):c.*1628C>G rs886052001
NM_032575.2(GLIS2):c.*1700G>A rs886052002
NM_032575.2(GLIS2):c.*173G>A rs139029261
NM_032575.2(GLIS2):c.*1761C>T rs370625022
NM_032575.2(GLIS2):c.*1791T>C rs886052003
NM_032575.2(GLIS2):c.*1826C>T rs757541
NM_032575.2(GLIS2):c.*1830C>T rs578236633
NM_032575.2(GLIS2):c.*1988A>G rs139152543
NM_032575.2(GLIS2):c.*232T>G rs114705511
NM_032575.2(GLIS2):c.*23G>A rs146555568
NM_032575.2(GLIS2):c.*278C>T rs116692282
NM_032575.2(GLIS2):c.*291_*293TCC[1] rs377612419
NM_032575.2(GLIS2):c.*2C>T rs144489623
NM_032575.2(GLIS2):c.*399T>G rs189481658
NM_032575.2(GLIS2):c.*437A>C rs533863589
NM_032575.2(GLIS2):c.*43G>A rs184772323
NM_032575.2(GLIS2):c.*525C>T rs886051991
NM_032575.2(GLIS2):c.*54C>T rs368483996
NM_032575.2(GLIS2):c.*551C>G rs886051992
NM_032575.2(GLIS2):c.*611G>A rs886051993
NM_032575.2(GLIS2):c.*614G>A rs653539
NM_032575.2(GLIS2):c.*632G>A rs886051994
NM_032575.2(GLIS2):c.*712C>G rs886051995
NM_032575.2(GLIS2):c.*762C>T rs573926229
NM_032575.2(GLIS2):c.*796G>C rs111818339
NM_032575.2(GLIS2):c.*856C>T rs886051996
NM_032575.2(GLIS2):c.*881C>T rs540618522
NM_032575.2(GLIS2):c.*887G>C rs886051997
NM_032575.2(GLIS2):c.*916G>A rs72766567
NM_032575.2(GLIS2):c.-11G>A rs28449480
NM_032575.2(GLIS2):c.1010C>T (p.Pro337Leu) rs140544340
NM_032575.2(GLIS2):c.1011G>A (p.Pro337=) rs200814551
NM_032575.2(GLIS2):c.101G>A (p.Arg34His)
NM_032575.2(GLIS2):c.1105G>A (p.Gly369Ser) rs200720013
NM_032575.2(GLIS2):c.1128C>T (p.Pro376=) rs750906253
NM_032575.2(GLIS2):c.1180G>A (p.Gly394Ser) rs775114398
NM_032575.2(GLIS2):c.1194_1208dup (p.Gly401_Pro405dup) rs878855164
NM_032575.2(GLIS2):c.1259C>T (p.Pro420Leu) rs75495782
NM_032575.2(GLIS2):c.1273G>A (p.Gly425Arg) rs199849300
NM_032575.2(GLIS2):c.127G>A (p.Val43Met) rs886051989
NM_032575.2(GLIS2):c.1311A>C (p.Ala437=) rs3810817
NM_032575.2(GLIS2):c.1326C>T (p.Ala442=) rs767819594
NM_032575.2(GLIS2):c.1335G>C (p.Glu445Asp) rs761985295
NM_032575.2(GLIS2):c.1350G>A (p.Ser450=) rs150464446
NM_032575.2(GLIS2):c.1355C>A (p.Pro452His) rs776535774
NM_032575.2(GLIS2):c.1388C>T (p.Thr463Met)
NM_032575.2(GLIS2):c.1403C>T (p.Thr468Met) rs138285254
NM_032575.2(GLIS2):c.1413C>G (p.Ser471Arg) rs201182025
NM_032575.2(GLIS2):c.1431C>T (p.Pro477=) rs150810544
NM_032575.2(GLIS2):c.1464G>A (p.Leu488=) rs149580171
NM_032575.2(GLIS2):c.1474A>G (p.Thr492Ala) rs8057701
NM_032575.2(GLIS2):c.1476G>A (p.Thr492=) rs140403969
NM_032575.2(GLIS2):c.1539G>A (p.Pro513=) rs769088578
NM_032575.2(GLIS2):c.1569G>A (p.Val523=) rs371022001
NM_032575.2(GLIS2):c.18G>A (p.Glu6=) rs759679058
NM_032575.2(GLIS2):c.210G>A (p.Glu70=) rs886051990
NM_032575.2(GLIS2):c.223G>T (p.Ala75Ser) rs72766563
NM_032575.2(GLIS2):c.239A>T (p.Asp80Val) rs144447862
NM_032575.2(GLIS2):c.291G>A (p.Ser97=) rs529581775
NM_032575.2(GLIS2):c.344C>T (p.Ser115Leu) rs771450245
NM_032575.2(GLIS2):c.415G>A (p.Gly139Arg) rs147175353
NM_032575.2(GLIS2):c.505G>A (p.Val169Met) rs144844035
NM_032575.2(GLIS2):c.523T>C (p.Cys175Arg) rs587777353
NM_032575.2(GLIS2):c.627C>T (p.Cys209=) rs746571582
NM_032575.2(GLIS2):c.651C>T (p.Asn217=) rs140609747
NM_032575.2(GLIS2):c.693C>T (p.Asn231=) rs150071733
NM_032575.2(GLIS2):c.70C>A (p.Arg24=) rs34543395
NM_032575.2(GLIS2):c.747C>T (p.Asn249=) rs763296256
NM_032575.2(GLIS2):c.775+1G>T rs878855335
NM_032575.2(GLIS2):c.864T>C (p.Tyr288=) rs669561
NM_032575.2(GLIS2):c.894C>T (p.Pro298=) rs112926217

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