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: rs13333226
rs13333226
0.827 0.200 16 20354332 intron variant A/G snv 0.23
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.810 1.000 2 2010 2016
dbSNP: rs12917707
rs12917707
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.800 1.000 1 2013 2016
dbSNP: rs4293393
rs4293393
0.827 0.200 16 20353266 intron variant A/G snv 0.20
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.800 1.000 1 2010 2010
dbSNP: rs12917707
rs12917707
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.720 1.000 3 2009 2015
dbSNP: rs13333226
rs13333226
0.827 0.200 16 20354332 intron variant A/G snv 0.23
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.710 1.000 1 2011 2018
dbSNP: rs13333226
rs13333226
0.827 0.200 16 20354332 intron variant A/G snv 0.23
CUI: C0011847
Disease: Diabetes
Diabetes
0.710 1.000 1 2011 2018
dbSNP: rs12917707
rs12917707
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14
Creatinine measurement, serum (procedure)
0.700 1.000 2 2010 2016
dbSNP: rs13329952
rs13329952
1.000 0.080 16 20355185 intron variant T/C snv 0.24
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 2 2016 2019
dbSNP: rs12917707
rs12917707
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14
CUI: C0011847
Disease: Diabetes
Diabetes
0.700 1.000 1 2016 2016
dbSNP: rs12917707
rs12917707
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.700 1.000 1 2016 2016
dbSNP: rs12922822
rs12922822
1.000 0.040 16 20356323 upstream gene variant C/A;T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs12922822
rs12922822
1.000 0.040 16 20356323 upstream gene variant C/A;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.700 1.000 1 2019 2019
dbSNP: rs12922822
rs12922822
1.000 0.040 16 20356323 upstream gene variant C/A;T snv
CUI: C4280669
Disease: Velopharyngeal dysfunction
Velopharyngeal dysfunction
0.700 1.000 1 2018 2018
dbSNP: rs12922822
rs12922822
1.000 0.040 16 20356323 upstream gene variant C/A;T snv
CUI: C0011847
Disease: Diabetes
Diabetes
0.700 1.000 1 2019 2019
dbSNP: rs13329952
rs13329952
1.000 0.080 16 20355185 intron variant T/C snv 0.24
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2016 2016
dbSNP: rs13329952
rs13329952
1.000 0.080 16 20355185 intron variant T/C snv 0.24
Creatinine measurement, serum (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs13333226
rs13333226
0.827 0.200 16 20354332 intron variant A/G snv 0.23
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2018 2018
dbSNP: rs13333226
rs13333226
0.827 0.200 16 20354332 intron variant A/G snv 0.23
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2017 2017
dbSNP: rs13333226
rs13333226
0.827 0.200 16 20354332 intron variant A/G snv 0.23
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2018 2018
dbSNP: rs143583842
rs143583842
1.000 0.040 16 20341262 missense variant G/A;T snv 7.4E-04; 1.2E-05
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia
0.700 1.000 1 2018 2018
dbSNP: rs143583842
rs143583842
1.000 0.040 16 20341262 missense variant G/A;T snv 7.4E-04; 1.2E-05
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2018 2018
dbSNP: rs188709583
rs188709583
1.000 16 20337383 missense variant C/A;T snv 4.0E-06; 1.3E-04
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2018 2018
dbSNP: rs188709583
rs188709583
1.000 16 20337383 missense variant C/A;T snv 4.0E-06; 1.3E-04
Creatinine measurement, serum (procedure)
0.700 1.000 1 2018 2018
dbSNP: rs201761378
rs201761378
1.000 0.080 16 20341292 missense variant C/T snv 9.7E-04 2.4E-04
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2018 2018
dbSNP: rs4997081
rs4997081
16 20353912 intron variant G/C snv 0.25
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2019 2019