Source: GWASDB

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: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 1 2011 2019
dbSNP: rs968567
rs968567
0.851 0.240 11 61828092 intron variant C/T snv 0.11
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.810 1.000 2 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 3 2008 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 3 2009 2019
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 2 2010 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
High density lipoprotein measurement
0.800 1.000 2 2010 2012
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 1 2010 2019
dbSNP: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2010 2010
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE
0.800 1.000 1 2010 2010
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 1 2009 2019
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.800 1.000 1 2011 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
High density lipoprotein measurement
0.800 1.000 1 2009 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 1 2012 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.800 1.000 1 2011 2016
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: rs174549
rs174549
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26
CUI: C0018810
Disease: heart rate
heart rate
0.800 1.000 1 2013 2013
dbSNP: rs174550
rs174550
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 1.000 1 2012 2012
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 1 2010 2015
dbSNP: rs174548
rs174548
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.710 1.000 1 2011 2017
dbSNP: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 3 2009 2013
dbSNP: rs174548
rs174548
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 3 2008 2013
dbSNP: rs174545
rs174545
1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2010 2013
dbSNP: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013