ClinVar Miner

List of variants in gene GLIS2 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP
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.*1161G>A rs78428657
NM_001318918.1(GLIS2):c.*12G>A rs201860422
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.*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.*291_*293TCC[1] rs377612419
NM_001318918.1(GLIS2):c.*2C>T rs144489623
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.*551C>G rs886051992
NM_001318918.1(GLIS2):c.*611G>A rs886051993
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.*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.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.1273G>A (p.Gly425Arg) rs199849300
NM_001318918.1(GLIS2):c.127G>A (p.Val43Met) rs886051989
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.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.1431C>T (p.Pro477=) rs150810544
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.210G>A (p.Glu70=) rs886051990
NM_001318918.1(GLIS2):c.239A>T (p.Asp80Val) rs144447862
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.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_032575.3(GLIS2):c.*1095G>A
NM_032575.3(GLIS2):c.*1150C>T
NM_032575.3(GLIS2):c.*125G>A
NM_032575.3(GLIS2):c.*1319A>G
NM_032575.3(GLIS2):c.*1553G>A
NM_032575.3(GLIS2):c.*1710C>A
NM_032575.3(GLIS2):c.*1911G>C
NM_032575.3(GLIS2):c.*1931C>G
NM_032575.3(GLIS2):c.*1998C>G
NM_032575.3(GLIS2):c.*199G>A
NM_032575.3(GLIS2):c.*2021C>T
NM_032575.3(GLIS2):c.*204G>A
NM_032575.3(GLIS2):c.*2058G>A
NM_032575.3(GLIS2):c.*516C>T
NM_032575.3(GLIS2):c.*663C>G
NM_032575.3(GLIS2):c.*757G>A
NM_032575.3(GLIS2):c.*849G>C
NM_032575.3(GLIS2):c.*902C>T
NM_032575.3(GLIS2):c.1033G>A (p.Gly345Ser)
NM_032575.3(GLIS2):c.1040A>C (p.Tyr347Ser)
NM_032575.3(GLIS2):c.1177G>A (p.Gly393Arg)
NM_032575.3(GLIS2):c.1256C>T (p.Ser419Leu)
NM_032575.3(GLIS2):c.1510T>C (p.Leu504=)
NM_032575.3(GLIS2):c.1526T>G (p.Val509Gly)
NM_032575.3(GLIS2):c.346-4C>G
NM_032575.3(GLIS2):c.476C>T (p.Ser159Leu)
NM_032575.3(GLIS2):c.479C>G (p.Pro160Arg)
NM_032575.3(GLIS2):c.523-9C>T
NM_032575.3(GLIS2):c.546G>A (p.Leu182=)
NM_032575.3(GLIS2):c.56C>T (p.Ala19Val)
NM_032575.3(GLIS2):c.801C>T (p.Tyr267=)
NM_032575.3(GLIS2):c.903C>T (p.His301=)
NM_032575.3(GLIS2):c.995G>A (p.Arg332His)

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