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: rs174548
rs174548
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs174548
rs174548
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2010 2019
dbSNP: rs174548
rs174548
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2008 2008
dbSNP: rs174548
rs174548
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.700 1.000 1 2018 2018
dbSNP: rs174548
rs174548
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
Low density lipoprotein cholesterol measurement
0.800 1.000 1 2012 2019
dbSNP: rs174548
rs174548
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs174548
rs174548
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2018 2018
dbSNP: rs174548
rs174548
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs174548
rs174548
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
High density lipoprotein measurement
0.800 1.000 1 2010 2012
dbSNP: rs174557
rs174557
1.000 0.080 11 61813896 intron variant A/C;G;T snv
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.700 1.000 1 2018 2018
dbSNP: rs174557
rs174557
1.000 0.080 11 61813896 intron variant A/C;G;T snv
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2018 2018
dbSNP: rs174567
rs174567
1.000 0.080 11 61825533 intron variant A/G;T snv
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.700 1.000 1 2018 2018
dbSNP: rs174567
rs174567
1.000 0.080 11 61825533 intron variant A/G;T snv
CUI: C0523829
Disease: Phosphatidylcholine measurement
Phosphatidylcholine measurement
0.700 1.000 1 2019 2019
dbSNP: rs174567
rs174567
1.000 0.080 11 61825533 intron variant A/G;T snv
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2018 2018
dbSNP: rs174567
rs174567
1.000 0.080 11 61825533 intron variant A/G;T snv
CUI: C0242216
Disease: Biliary calculi
Biliary calculi
0.700 1.000 1 2018 2018
dbSNP: rs174568
rs174568
1.000 0.080 11 61826344 missense variant C/A;T snv 0.37
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2019 2019
dbSNP: rs174568
rs174568
1.000 0.080 11 61826344 missense variant C/A;T snv 0.37
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2018 2018
dbSNP: rs174568
rs174568
1.000 0.080 11 61826344 missense variant C/A;T snv 0.37
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.700 1.000 1 2018 2018
dbSNP: rs28456
rs28456
0.925 0.120 11 61822009 intron variant A/C;G snv
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.700 1.000 1 2018 2018
dbSNP: rs28456
rs28456
0.925 0.120 11 61822009 intron variant A/C;G snv
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2018 2018
dbSNP: rs28456
rs28456
0.925 0.120 11 61822009 intron variant A/C;G snv
CUI: C0202171
Disease: Phosphatidylinositol measurement
Phosphatidylinositol measurement
0.700 1.000 1 2019 2019
dbSNP: rs28456
rs28456
0.925 0.120 11 61822009 intron variant A/C;G snv
CUI: C0523829
Disease: Phosphatidylcholine measurement
Phosphatidylcholine measurement
0.700 1.000 1 2019 2019
dbSNP: rs28456
rs28456
0.925 0.120 11 61822009 intron variant A/C;G snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.710 1.000 1 2018 2018
dbSNP: rs57668028
rs57668028
1.000 0.080 11 61824524 intron variant AA/-;AAA;AAAA delins 7.5E-03
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.700 1.000 1 2018 2018
dbSNP: rs57668028
rs57668028
1.000 0.080 11 61824524 intron variant AA/-;AAA;AAAA delins 7.5E-03
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2018 2018