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: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
High density lipoprotein measurement
0.800 1.000 7 2010 2019
dbSNP: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
Low density lipoprotein cholesterol measurement
0.800 1.000 6 2009 2019
dbSNP: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 6 2008 2019
dbSNP: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2010 2019
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
High density lipoprotein measurement
0.800 1.000 4 2009 2019
dbSNP: rs174551
rs174551
11 61806212 5 prime UTR variant T/C snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 4 2018 2019
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2009 2019
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 3 2016 2019
dbSNP: rs174550
rs174550
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
0.800 1.000 3 2010 2015
dbSNP: rs174551
rs174551
11 61806212 5 prime UTR variant T/C snv 0.28
Low density lipoprotein cholesterol measurement
0.700 1.000 3 2015 2019
dbSNP: rs174554
rs174554
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 3 2015 2019
dbSNP: rs1535
rs1535
0.752 0.240 11 61830500 intron variant A/G snv 0.31
High density lipoprotein measurement
0.800 1.000 2 2010 2019
dbSNP: rs1535
rs1535
0.752 0.240 11 61830500 intron variant A/G snv 0.31
Low density lipoprotein cholesterol measurement
0.800 1.000 2 2012 2019
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0523744
Disease: Lipids measurement
Lipids measurement
0.800 1.000 2 2012 2016
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: rs174549
rs174549
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 2 2016 2019
dbSNP: rs174550
rs174550
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28
High density lipoprotein measurement
0.700 1.000 2 2017 2018
dbSNP: rs174550
rs174550
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2017 2018
dbSNP: rs174551
rs174551
11 61806212 5 prime UTR variant T/C snv 0.28
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs174551
rs174551
11 61806212 5 prime UTR variant T/C snv 0.28
High density lipoprotein measurement
0.700 1.000 2 2018 2019
dbSNP: rs174554
rs174554
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28
Low density lipoprotein cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs174554
rs174554
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2019
dbSNP: rs174554
rs174554
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28
High density lipoprotein measurement
0.700 1.000 2 2018 2019
dbSNP: rs174559
rs174559
11 61814184 non coding transcript exon variant G/A snv 0.23
Red cell distribution width determination
0.700 1.000 2 2017 2019