ClinVar Miner

List of variants in gene GLIS3 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: 127
Download table as spreadsheet
HGVS dbSNP
NM_001042413.2(GLIS3):c.*1002T>C rs574929091
NM_001042413.2(GLIS3):c.*1152T>G rs1331260
NM_001042413.2(GLIS3):c.*1197G>C rs10973690
NM_001042413.2(GLIS3):c.*1286G>A rs115457453
NM_001042413.2(GLIS3):c.*1416G>T rs775321147
NM_001042413.2(GLIS3):c.*1562A>C rs12376878
NM_001042413.2(GLIS3):c.*1602T>G rs80030970
NM_001042413.2(GLIS3):c.*1636G>T rs183582256
NM_001042413.2(GLIS3):c.*1686T>A rs886063947
NM_001042413.2(GLIS3):c.*1744A>G rs886063946
NM_001042413.2(GLIS3):c.*1760T>G rs116077269
NM_001042413.2(GLIS3):c.*1800_*1801insC rs34028765
NM_001042413.2(GLIS3):c.*1827T>G rs16919705
NM_001042413.2(GLIS3):c.*1832A>G rs10116901
NM_001042413.2(GLIS3):c.*1901G>C rs755453024
NM_001042413.2(GLIS3):c.*1999_*2000CT[1] rs567458278
NM_001042413.2(GLIS3):c.*2052C>A rs151287182
NM_001042413.2(GLIS3):c.*2113G>T rs886063945
NM_001042413.2(GLIS3):c.*2185G>A rs374555254
NM_001042413.2(GLIS3):c.*2191G>A rs3739618
NM_001042413.2(GLIS3):c.*2326C>T rs3739619
NM_001042413.2(GLIS3):c.*2411A>G rs368160002
NM_001042413.2(GLIS3):c.*2460C>T rs1053277
NM_001042413.2(GLIS3):c.*2499T>A rs886063944
NM_001042413.2(GLIS3):c.*2673dup rs147364042
NM_001042413.2(GLIS3):c.*2707T>G rs76838287
NM_001042413.2(GLIS3):c.*2732G>A rs1053280
NM_001042413.2(GLIS3):c.*2806G>A rs12351289
NM_001042413.2(GLIS3):c.*2813C>T rs77896717
NM_001042413.2(GLIS3):c.*2828A>C rs886063943
NM_001042413.2(GLIS3):c.*2840dup rs142133114
NM_001042413.2(GLIS3):c.*2850C>G rs184008619
NM_001042413.2(GLIS3):c.*2856A>C rs147347517
NM_001042413.2(GLIS3):c.*2890C>G rs192113877
NM_001042413.2(GLIS3):c.*2914G>T rs185773873
NM_001042413.2(GLIS3):c.*2927T>G rs886063942
NM_001042413.2(GLIS3):c.*2944T>C rs2297324
NM_001042413.2(GLIS3):c.*2992C>T rs886063941
NM_001042413.2(GLIS3):c.*3012G>C rs35359206
NM_001042413.2(GLIS3):c.*3218A>C rs73640770
NM_001042413.2(GLIS3):c.*3231A>C rs886063940
NM_001042413.2(GLIS3):c.*3257A>G rs117876027
NM_001042413.2(GLIS3):c.*3330G>A rs886063939
NM_001042413.2(GLIS3):c.*3336A>T rs1455174
NM_001042413.2(GLIS3):c.*3336_*3337del rs66766243
NM_001042413.2(GLIS3):c.*3336_*3340del rs886063937
NM_001042413.2(GLIS3):c.*3336del rs200420290
NM_001042413.2(GLIS3):c.*3337_*3338insA rs886063938
NM_001042413.2(GLIS3):c.*3338T>A rs202199541
NM_001042413.2(GLIS3):c.*3339T>A rs868836548
NM_001042413.2(GLIS3):c.*3351_*3352del rs1554622288
NM_001042413.2(GLIS3):c.*3377del rs202118987
NM_001042413.2(GLIS3):c.*3409G>A rs115222174
NM_001042413.2(GLIS3):c.*3692A>T rs75958174
NM_001042413.2(GLIS3):c.*3776G>C rs552893696
NM_001042413.2(GLIS3):c.*391C>T rs886063951
NM_001042413.2(GLIS3):c.*3920G>A rs747590249
NM_001042413.2(GLIS3):c.*448G>A rs734752
NM_001042413.2(GLIS3):c.*572T>C rs886063950
NM_001042413.2(GLIS3):c.*663_*664dup rs5896025
NM_001042413.2(GLIS3):c.*664dup rs5896025
NM_001042413.2(GLIS3):c.*711C>G rs4997836
NM_001042413.2(GLIS3):c.*712C>T rs912257
NM_001042413.2(GLIS3):c.*818C>T rs886063949
NM_001042413.2(GLIS3):c.*963T>C rs886063948
NM_001042413.2(GLIS3):c.*969C>G rs756499534
NM_001042413.2(GLIS3):c.*99C>T rs886063952
NM_001042413.2(GLIS3):c.-110C>G rs568860551
NM_001042413.2(GLIS3):c.-115G>A rs886063958
NM_001042413.2(GLIS3):c.-131G>A rs7852293
NM_001042413.2(GLIS3):c.-154C>T rs533529459
NM_001042413.2(GLIS3):c.-165C>T rs886063959
NM_001042413.2(GLIS3):c.-223C>T rs746014906
NM_001042413.2(GLIS3):c.-270C>A rs73641408
NM_001042413.2(GLIS3):c.-344C>T rs762042518
NM_001042413.2(GLIS3):c.-345C>T rs886063960
NM_001042413.2(GLIS3):c.-514G>A rs146119120
NM_001042413.2(GLIS3):c.-523C>G rs547410899
NM_001042413.2(GLIS3):c.-524C>T rs567222677
NM_001042413.2(GLIS3):c.-588C>A rs886063961
NM_001042413.2(GLIS3):c.-619C>G rs886063962
NM_001042413.2(GLIS3):c.-636C>T rs377748184
NM_001042413.2(GLIS3):c.-641C>A rs886063963
NM_001042413.2(GLIS3):c.-681C>T rs138857227
NM_001042413.2(GLIS3):c.-79G>A rs886063956
NM_001042413.2(GLIS3):c.1044C>T (p.Tyr348=) rs146238548
NM_001042413.2(GLIS3):c.1056G>C (p.Leu352=) rs140880100
NM_001042413.2(GLIS3):c.105C>T (p.Ser35=) rs372340726
NM_001042413.2(GLIS3):c.1090C>T (p.Pro364Ser) rs143056249
NM_001042413.2(GLIS3):c.1126C>T (p.Pro376Ser) rs76342955
NM_001042413.2(GLIS3):c.1214C>T (p.Pro405Leu) rs764072714
NM_001042413.2(GLIS3):c.1216G>T (p.Gly406Cys) rs75462592
NM_001042413.2(GLIS3):c.125C>T (p.Pro42Leu) rs199506457
NM_001042413.2(GLIS3):c.1260C>T (p.Pro420=) rs377419083
NM_001042413.2(GLIS3):c.1270T>C (p.Ser424Pro) rs806052
NM_001042413.2(GLIS3):c.1327C>T (p.Leu443=) rs529418802
NM_001042413.2(GLIS3):c.1367C>A (p.Pro456Gln) rs6415788
NM_001042413.2(GLIS3):c.1368A>T (p.Pro456=) rs755087869
NM_001042413.2(GLIS3):c.141G>A (p.Ser47=) rs201142941
NM_001042413.2(GLIS3):c.1452G>A (p.Gln484=) rs143229804
NM_001042413.2(GLIS3):c.1526C>T (p.Ala509Val) rs776030305
NM_001042413.2(GLIS3):c.1536C>A (p.Asp512Glu) rs148199056
NM_001042413.2(GLIS3):c.1608C>G (p.Cys536Trp) rs879255608
NM_001042413.2(GLIS3):c.1681C>T (p.His561Tyr) rs868197660
NM_001042413.2(GLIS3):c.171C>T (p.Asn57=) rs117802495
NM_001042413.2(GLIS3):c.1723G>A (p.Glu575Lys) rs780390959
NM_001042413.2(GLIS3):c.1881T>C (p.Tyr627=) rs141985853
NM_001042413.2(GLIS3):c.1988G>A (p.Arg663Gln) rs144720690
NM_001042413.2(GLIS3):c.2027G>T (p.Cys676Phe) rs149983395
NM_001042413.2(GLIS3):c.2060C>T (p.Ser687Phe) rs374929970
NM_001042413.2(GLIS3):c.2110G>A (p.Gly704Arg) rs886063953
NM_001042413.2(GLIS3):c.2129-1G>C rs1563806466
NM_001042413.2(GLIS3):c.2297+11_2297+12del rs779433100
NM_001042413.2(GLIS3):c.2323C>T (p.His775Tyr) rs745671153
NM_001042413.2(GLIS3):c.2338dup (p.Arg780fs) rs869320723
NM_001042413.2(GLIS3):c.2686C>T (p.Leu896Phe) rs76094493
NM_001042413.2(GLIS3):c.2710G>A (p.Gly904Arg) rs150310830
NM_001042413.2(GLIS3):c.2745C>T (p.Thr915=) rs377426046
NM_001042413.2(GLIS3):c.287C>G (p.Pro96Arg) rs143425492
NM_001042413.2(GLIS3):c.496C>G (p.Pro166Ala) rs141467694
NM_001042413.2(GLIS3):c.571_572dup (p.Leu191_Asn192insTer)
NM_001042413.2(GLIS3):c.638G>A (p.Ser213Asn) rs748030278
NM_001042413.2(GLIS3):c.82A>G (p.Ile28Val) rs113754532
NM_001042413.2(GLIS3):c.844C>G (p.Pro282Ala) rs143051164
NM_001042413.2(GLIS3):c.893C>A (p.Ser298Tyr) rs148572278
NM_001042413.2(GLIS3):c.932del (p.Gly311fs) rs879255609
NM_001042413.2(GLIS3):c.954C>T (p.Thr318=) rs75564360

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.