ClinVar Miner

List of variants in gene GLIS3 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_001042413.2(GLIS3):c.1270T>C (p.Ser424Pro) rs806052 0.99890
NM_001042413.2(GLIS3):c.*1800_*1801insC rs34028765 0.96678
NM_001042413.2(GLIS3):c.*2460C>T rs1053277 0.95364
NM_001042413.2(GLIS3):c.*712C>T rs912257 0.95023
NM_001042413.2(GLIS3):c.*2732G>A rs1053280 0.84277
NM_001042413.2(GLIS3):c.1367C>A (p.Pro456Gln) rs6415788 0.62075
NM_001042413.2(GLIS3):c.*1197G>C rs10973690 0.39299
NM_001042413.2(GLIS3):c.*1152T>G rs1331260 0.39087
NM_001042413.2(GLIS3):c.*1562A>C rs12376878 0.38632
NM_001042413.2(GLIS3):c.*3336A>T rs1455174 0.30904
NM_001042413.2(GLIS3):c.*448G>A rs734752 0.26355
NM_001042413.2(GLIS3):c.*2191G>A rs3739618 0.20986
NM_001042413.2(GLIS3):c.*1832A>G rs10116901 0.09872
NM_001042413.2(GLIS3):c.*1602T>G rs80030970 0.08524
NM_001042413.2(GLIS3):c.*3012G>C rs35359206 0.08281
NM_001042413.2(GLIS3):c.*711C>G rs4997836 0.07855
NM_001042413.2(GLIS3):c.*3409G>A rs115222174 0.05308
NM_001042413.2(GLIS3):c.*3692A>T rs75958174 0.04783
NM_001042413.2(GLIS3):c.2686C>T (p.Leu896Phe) rs76094493 0.03919
NM_001042413.2(GLIS3):c.*2944T>C rs2297324 0.03830
NM_001042413.2(GLIS3):c.*2813C>T rs77896717 0.03600
NM_001042413.2(GLIS3):c.*2806G>A rs12351289 0.03061
NM_001042413.2(GLIS3):c.-681C>T rs138857227 0.02897
NM_001042413.2(GLIS3):c.*3218A>C rs73640770 0.02215
NM_001042413.2(GLIS3):c.*1827T>G rs16919705 0.01953
NM_001042413.2(GLIS3):c.*3257A>G rs117876027 0.01860
NM_001042413.2(GLIS3):c.1536C>A (p.Asp512Glu) rs148199056 0.01645
NM_001042413.2(GLIS3):c.938G>C (p.Gly313Ala) rs35154632 0.01104
NM_001042413.2(GLIS3):c.171C>T (p.Asn57=) rs117802495 0.00947
NM_001042413.2(GLIS3):c.1216G>T (p.Gly406Cys) rs75462592 0.00898
NM_001042413.2(GLIS3):c.*1760T>G rs116077269 0.00871
NM_001042413.2(GLIS3):c.*2856A>C rs147347517 0.00826
NM_001042413.2(GLIS3):c.1126C>T (p.Pro376Ser) rs76342955 0.00811
NM_001042413.2(GLIS3):c.*1232T>G rs114506692 0.00658
NM_001042413.2(GLIS3):c.1881T>C (p.Tyr627=) rs141985853 0.00500
NM_001042413.2(GLIS3):c.-524C>T rs567222677 0.00278
NM_001042413.2(GLIS3):c.*2326C>T rs3739619 0.00063
NM_001042413.2(GLIS3):c.1260C>T (p.Pro420=) rs377419083 0.00059
NM_001042413.2(GLIS3):c.-636C>T rs377748184 0.00044
NM_001042413.2(GLIS3):c.1327C>T (p.Leu443=) rs529418802 0.00022
NM_001042413.2(GLIS3):c.2723C>T (p.Ala908Val) rs140101069 0.00008
NM_001042413.2(GLIS3):c.*2891G>C rs3025
NM_001042413.2(GLIS3):c.*3336_*3337del rs66766243
NM_001042413.2(GLIS3):c.*664dup rs5896025
NM_001042413.2(GLIS3):c.-131G>A rs7852293
NM_001042413.2(GLIS3):c.-270C>A rs73641408
NM_001042413.2(GLIS3):c.1085C>A (p.Pro362Gln) rs146131512
NM_001042413.2(GLIS3):c.2471A>G (p.His824Arg) rs140981222

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