ClinVar Miner

List of variants in gene GLIS3 reported as likely benign for digestive system disorder

Included ClinVar conditions (605):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_001042413.2(GLIS3):c.1216G>T (p.Gly406Cys) rs75462592 0.00898
NM_001042413.2(GLIS3):c.*2034T>C rs193108375 0.00334
NM_001042413.2(GLIS3):c.1318A>G (p.Thr440Ala) rs80161424 0.00314
NM_001042413.2(GLIS3):c.1545G>C (p.Glu515Asp) rs72687988 0.00304
NM_001042413.2(GLIS3):c.*2707T>G rs76838287 0.00282
NM_001042413.2(GLIS3):c.2089G>A (p.Val697Met) rs148816140 0.00229
NM_001042413.2(GLIS3):c.893C>A (p.Ser298Tyr) rs148572278 0.00199
NM_001042413.2(GLIS3):c.*2404A>C rs569350667 0.00183
NM_001042413.2(GLIS3):c.232C>G (p.Arg78Gly) rs148168366 0.00178
NM_001042413.2(GLIS3):c.1092G>T (p.Pro364=) rs74680081 0.00172
NM_001042413.2(GLIS3):c.1090C>T (p.Pro364Ser) rs143056249 0.00165
NM_001042413.2(GLIS3):c.954C>T (p.Thr318=) rs75564360 0.00165
NM_001042413.2(GLIS3):c.1191G>C (p.Gln397His) rs138497710 0.00163
NM_001042413.2(GLIS3):c.1767G>T (p.Arg589=) rs138100080 0.00160
NM_001042413.2(GLIS3):c.496C>G (p.Pro166Ala) rs141467694 0.00147
NM_001042413.2(GLIS3):c.*2787G>A rs187613528 0.00141
NM_001042413.2(GLIS3):c.*2850C>G rs184008619 0.00140
NM_001042413.2(GLIS3):c.*1116G>A rs150411858 0.00139
NM_001042413.2(GLIS3):c.2340G>A (p.Arg780=) rs147473975 0.00086
NM_001042413.2(GLIS3):c.744A>G (p.Leu248=) rs139080385 0.00086
NM_001042413.2(GLIS3):c.*557A>G rs75480480 0.00085
NM_001042413.2(GLIS3):c.1199A>G (p.His400Arg) rs376031632 0.00081
NM_001042413.2(GLIS3):c.1260C>T (p.Pro420=) rs377419083 0.00059
NM_001042413.2(GLIS3):c.1200C>G (p.His400Gln) rs374943049 0.00026
NM_001042413.2(GLIS3):c.2421C>G (p.Ser807=) rs563920093 0.00026
NM_001042413.2(GLIS3):c.*673T>C rs2380903 0.00023
NM_001042413.2(GLIS3):c.1327C>T (p.Leu443=) rs529418802 0.00022
NM_001042413.2(GLIS3):c.-523C>G rs547410899 0.00019
NM_001042413.2(GLIS3):c.89C>T (p.Ala30Val) rs114010705 0.00018
NM_001042413.2(GLIS3):c.1326C>T (p.Asp442=) rs758928731 0.00010
NM_001042413.2(GLIS3):c.1984-16C>T rs145670205 0.00008
NM_001042413.2(GLIS3):c.1686T>G (p.Ser562=) rs745836279 0.00007
NM_001042413.2(GLIS3):c.1395T>C (p.His465=) rs752606768 0.00006
NM_001042413.2(GLIS3):c.2297+16T>C rs377104078 0.00005
NM_001042413.2(GLIS3):c.*3601C>A rs553410195 0.00004
NM_001042413.2(GLIS3):c.*1166G>A rs371759528 0.00003
NM_001042413.2(GLIS3):c.*1636G>T rs183582256 0.00003
NM_001042413.2(GLIS3):c.1263C>T (p.Asp421=) rs755713904 0.00003
NM_001042413.2(GLIS3):c.1272G>A (p.Ser424=) rs764287243 0.00001
NM_001042413.2(GLIS3):c.1973C>G (p.Ala658Gly) rs977500969 0.00001
NM_001042413.2(GLIS3):c.555A>C (p.Ala185=) rs752433935 0.00001
NM_001042413.2(GLIS3):c.*2673dup rs147364042
NM_001042413.2(GLIS3):c.*2840dup rs142133114
NM_001042413.2(GLIS3):c.*2890C>G rs192113877
NM_001042413.2(GLIS3):c.*3189C>T rs548564187
NM_001042413.2(GLIS3):c.*3377del rs202118987
NM_001042413.2(GLIS3):c.*663_*664dup rs5896025
NM_001042413.2(GLIS3):c.1085C>A (p.Pro362Gln) rs146131512
NM_001042413.2(GLIS3):c.1327C>G (p.Leu443Val) rs529418802
NM_001042413.2(GLIS3):c.2473+13C>T rs368773221
NM_001042413.2(GLIS3):c.2657-17C>T rs746005781
NM_001042413.2(GLIS3):c.844C>G (p.Pro282Ala) rs143051164

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