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: rs10032549
rs10032549
4 76476862 intron variant A/G snv 0.43
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.800 1.000 1 2013 2013
dbSNP: rs13146355
rs13146355
1.000 0.040 4 76490987 intron variant G/A snv 0.33
CUI: C0373675
Disease: Magnesium measurement
Magnesium measurement
0.800 1.000 1 2010 2010
dbSNP: rs17319721
rs17319721
0.925 0.080 4 76447694 intron variant G/A snv 0.34
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.800 1.000 1 2013 2016
dbSNP: rs4859682
rs4859682
4 76489165 intron variant C/A snv 0.33
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.800 1.000 1 2013 2013
dbSNP: rs13146355
rs13146355
1.000 0.040 4 76490987 intron variant G/A snv 0.33
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 3 2017 2019
dbSNP: rs13146355
rs13146355
1.000 0.040 4 76490987 intron variant G/A snv 0.33
Creatinine measurement, serum (procedure)
0.700 1.000 2 2017 2019
dbSNP: rs17319721
rs17319721
0.925 0.080 4 76447694 intron variant G/A snv 0.34
Creatinine measurement, serum (procedure)
0.700 1.000 2 2010 2016
dbSNP: rs10008637
rs10008637
4 76492991 intron variant T/A;C snv 0.35
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs10008637
rs10008637
4 76492991 intron variant T/A;C snv 0.35
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs10023335
rs10023335
4 76437834 intron variant T/C snv 0.29
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria
0.700 1.000 1 2019 2019
dbSNP: rs10050141
rs10050141
1.000 0.040 4 76530384 intron variant G/A snv 9.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs1013105
rs1013105
4 76687512 intron variant G/A;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs111449836
rs111449836
4 76480299 intron variant C/T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs12500824
rs12500824
1.000 0.040 4 76495474 intron variant A/G;T snv
Alanine aminotransferase measurement
0.700 1.000 1 2018 2018
dbSNP: rs12500824
rs12500824
1.000 0.040 4 76495474 intron variant A/G;T snv
Serum Alanine Aminotransferase Measurement
0.700 1.000 1 2018 2018
dbSNP: rs12500824
rs12500824
1.000 0.040 4 76495474 intron variant A/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2018 2018
dbSNP: rs13105942
rs13105942
1.000 0.040 4 76527447 intron variant G/A snv 7.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs13146355
rs13146355
1.000 0.040 4 76490987 intron variant G/A snv 0.33
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs13146355
rs13146355
1.000 0.040 4 76490987 intron variant G/A snv 0.33
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.700 1.000 1 2019 2019
dbSNP: rs13146355
rs13146355
1.000 0.040 4 76490987 intron variant G/A snv 0.33
CUI: C0011847
Disease: Diabetes
Diabetes
0.700 1.000 1 2019 2019
dbSNP: rs13151434
rs13151434
1.000 0.040 4 76527046 intron variant G/A snv 6.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs143141511
rs143141511
4 76647838 intron variant G/A snv 4.2E-03
CUI: C2697758
Disease: Interleukin 10 Measurement
Interleukin 10 Measurement
0.700 1.000 1 2017 2017
dbSNP: rs148172770
rs148172770
4 76730805 missense variant C/T snv 1.3E-04 3.4E-04
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2018 2018
dbSNP: rs17319721
rs17319721
0.925 0.080 4 76447694 intron variant G/A snv 0.34
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2010 2010
dbSNP: rs1986734
rs1986734
1.000 0.120 4 76499631 intron variant C/T snv 0.43
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.700 1.000 1 2016 2016