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: 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: 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: 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: 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: rs7047871
rs7047871
GLIS3
9 4050113 intron variant T/A snv 0.30
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2019 2019
dbSNP: rs6415788
rs6415788
GLIS3
9 4118111 missense variant G/T snv 0.67 0.62
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 2 2016 2019
dbSNP: rs6415788
rs6415788
GLIS3
9 4118111 missense variant G/T snv 0.67 0.62
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs6415788
rs6415788
GLIS3
9 4118111 missense variant G/T snv 0.67 0.62
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs6415788
rs6415788
GLIS3
9 4118111 missense variant G/T snv 0.67 0.62
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
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: 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: rs7872188
rs7872188
GLIS3
9 4124377 intron variant C/T snv 0.36
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2017 2017
dbSNP: rs12336359
rs12336359
GLIS3
9 4129657 intron variant G/C snv 0.37
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs10114763
rs10114763
GLIS3
1.000 0.040 9 4143749 intron variant A/T snv 0.39
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		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: rs7026684
rs7026684
GLIS3
9 4215308 intron variant G/A snv 0.39
CUI: C1720164
Disease: Central corneal thickness
Central corneal thickness 		0.700 1.000 1 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
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: 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: 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: rs10974399
rs10974399
GLIS3
9 4232588 intron variant G/T snv 0.40
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
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: rs10974406
rs10974406
GLIS3
9 4237041 intron variant T/C snv 0.29
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018