Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7034200
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.700 1.000 3 2010 2015
dbSNP: rs10116772
rs10116772
GLIS3
0.882 0.080 9 4290541 intron variant C/A;T snv
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		0.700 1.000 1 2018 2018
dbSNP: rs10116772
rs10116772
GLIS3
0.882 0.080 9 4290541 intron variant C/A;T snv
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		0.700 1.000 1 2018 2018
dbSNP: rs1017568
rs1017568
GLIS3
1.000 0.080 9 3948365 intron variant T/C;G snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2018 2018
dbSNP: rs10974256
rs10974256
GLIS3
9 3952892 intron variant G/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1570203
rs1570203
GLIS3
9 4120648 intron variant G/A;C snv
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs1570203
rs1570203
GLIS3
9 4120648 intron variant G/A;C snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs1983753
rs1983753
GLIS3
9 4160364 intron variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs28558845
rs28558845
GLIS3
9 4334791 intron variant G/A;C;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs4237150
rs4237150
GLIS3
9 4290085 intron variant G/A;C;T snv
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.800 1.000 1 2012 2015
dbSNP: rs4741893
rs4741893
GLIS3
9 4123284 intron variant G/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs501461
rs501461
GLIS3
9 4039727 intron variant G/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs514716
rs514716
GLIS3
1.000 0.080 9 3929424 intron variant C/A;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.710 1.000 1 2013 2013
dbSNP: rs57884925
rs57884925
GLIS3
9 4285119 intron variant C/G;T snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2018 2018
dbSNP: rs57884925
rs57884925
GLIS3
9 4285119 intron variant C/G;T snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2018 2018
dbSNP: rs6476839
rs6476839
GLIS3
0.925 0.120 9 4290823 intron variant A/C;T snv
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs7020673
rs7020673
GLIS3
0.882 0.200 9 4291747 intron variant C/A;G snv
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.810 0.500 1 2009 2017
dbSNP: rs7034200
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.750 1.000 1 2011 2019
dbSNP: rs7034200
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.800 1.000 1 2012 2012
dbSNP: rs736893
rs736893
GLIS3
0.925 0.040 9 4217028 intron variant G/A;C snv
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma 		0.720 1.000 1 2016 2019
dbSNP: rs12348139
rs12348139
GLIS3
9 4232743 intron variant T/C snv 7.9E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs13301469
rs13301469
GLIS3
1.000 0.040 9 3911353 intron variant C/G snv 0.17
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2015 2015
dbSNP: rs10119187
rs10119187
GLIS3
9 4223660 intron variant T/C;G snv 0.22
CUI: C0202231
Disease: Thyroxine measurement
Thyroxine measurement 		0.700 1.000 1 2018 2018
dbSNP: rs6476827
rs6476827
GLIS3
9 4220832 intron variant C/G snv 0.24
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 2 2018 2018
dbSNP: rs1570204
rs1570204
GLIS3
9 4216751 intron variant T/C snv 0.25
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 2 2018 2018