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: rs1570204
rs1570204
9 4216751 intron variant T/C snv 0.25
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 2 2018 2018
dbSNP: rs6415788
rs6415788
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: rs6476827
rs6476827
9 4220832 intron variant C/G snv 0.24
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 2 2018 2018
dbSNP: rs10119187
rs10119187
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: rs10974256
rs10974256
9 3952892 intron variant G/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10974399
rs10974399
9 4232588 intron variant G/T snv 0.40
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10974406
rs10974406
9 4237041 intron variant T/C snv 0.29
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs12336359
rs12336359
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: rs12348139
rs12348139
9 4232743 intron variant T/C snv 7.9E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs1570203
rs1570203
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
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: rs1571583
rs1571583
9 4267209 intron variant A/G snv 0.77
Thyroid stimulating hormone measurement
0.800 1.000 1 2013 2013
dbSNP: rs1571583
rs1571583
9 4267209 intron variant A/G snv 0.77
CUI: C0441683
Disease: Hormone measurement
Hormone measurement
0.700 1.000 1 2013 2013
dbSNP: rs1983753
rs1983753
9 4160364 intron variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2224492
rs2224492
9 4237546 intron variant A/G snv 0.25
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2017 2017
dbSNP: rs28558845
rs28558845
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
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
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
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: rs57884925
rs57884925
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
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: rs6415788
rs6415788
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
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
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: rs7026684
rs7026684
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