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: rs28927680
rs28927680
11 116748357 3 prime UTR variant C/G,T snp 9.3E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 3 2008 2013
dbSNP: rs10790162
rs10790162
0.923 0.143 11 116768388 A/G snp 0.93
High density lipoprotein measurement
0.800 1 2011 2011
dbSNP: rs10790162
rs10790162
0.923 0.143 11 116768388 A/G snp 0.93
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1 2011 2011
dbSNP: rs11820589
rs11820589
1.000 0.036 11 116763146 missense variant G/A snp 7.8E-02 9.3E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1 2011 2011
dbSNP: rs11825181
rs11825181
11 116755542 intron variant G/A snp 9.5E-02
CUI: C1271104
Disease: Blood pressure finding
Blood pressure finding
0.800 1 2011 2011
dbSNP: rs11825181
rs11825181
11 116755542 intron variant G/A snp 9.5E-02
CUI: C1272641
Disease: Systemic arterial pressure
Systemic arterial pressure
0.800 1 2011 2011
dbSNP: rs11825181
rs11825181
11 116755542 intron variant G/A snp 9.5E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.800 1 2011 2011
dbSNP: rs180327
rs180327
11 116752943 intron variant C/T snp 0.58
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 2 2012 2012
dbSNP: rs28927680
rs28927680
11 116748357 3 prime UTR variant C/G,T snp 9.3E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 2 2012 2013
dbSNP: rs6589565
rs6589565
11 116769521 intron variant A/G snp 0.93
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 2 2012 2013
dbSNP: rs10488699
rs10488699
11 116761784 intron variant C/T snp 9.2E-02
CUI: C3549252
Disease: response to statin
response to statin
0.700 1 2011 2011
dbSNP: rs10790162
rs10790162
0.923 0.143 11 116768388 A/G snp 0.93
CUI: C3549252
Disease: response to statin
response to statin
0.700 1 2011 2011
dbSNP: rs10790162
rs10790162
0.923 0.143 11 116768388 A/G snp 0.93
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1 2012 2012
dbSNP: rs10790162
rs10790162
0.923 0.143 11 116768388 A/G snp 0.93
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement
0.700 1 2011 2011
dbSNP: rs11820589
rs11820589
1.000 0.036 11 116763146 missense variant G/A snp 7.8E-02 9.3E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1 2012 2012
dbSNP: rs11820589
rs11820589
1.000 0.036 11 116763146 missense variant G/A snp 7.8E-02 9.3E-02
High density lipoprotein measurement
0.700 1 2012 2012
dbSNP: rs11820589
rs11820589
1.000 0.036 11 116763146 missense variant G/A snp 7.8E-02 9.3E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1 2012 2012
dbSNP: rs11820589
rs11820589
1.000 0.036 11 116763146 missense variant G/A snp 7.8E-02 9.3E-02
CUI: C3549252
Disease: response to statin
response to statin
0.700 1 2011 2011
dbSNP: rs11825181
rs11825181
11 116755542 intron variant G/A snp 9.5E-02
CUI: C3549252
Disease: response to statin
response to statin
0.700 1 2011 2011
dbSNP: rs12292921
rs12292921
11 116751247 intron variant T/G snp 9.5E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1 2009 2009
dbSNP: rs12292921
rs12292921
11 116751247 intron variant T/G snp 9.5E-02
CUI: C2246682
Disease: response to vitamin
response to vitamin
0.700 1 2012 2012
dbSNP: rs12292921
rs12292921
11 116751247 intron variant T/G snp 9.5E-02
CUI: C3549252
Disease: response to statin
response to statin
0.700 1 2011 2011
dbSNP: rs12294259
rs12294259
11 116766430 intron variant C/T snp 0.10
CUI: C3549252
Disease: response to statin
response to statin
0.700 1 2011 2011
dbSNP: rs180327
rs180327
11 116752943 intron variant C/T snp 0.58
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1 2012 2012
dbSNP: rs180327
rs180327
11 116752943 intron variant C/T snp 0.58
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1 2012 2012