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 snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2008 2019
dbSNP: rs180327
rs180327
11 116752943 intron variant C/T snv 0.58
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2012 2012
dbSNP: rs28927680
rs28927680
11 116748357 3 prime UTR variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2012 2019
dbSNP: rs6589565
rs6589565
11 116769521 intron variant A/G snv 0.93
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2012 2012
dbSNP: rs11825181
rs11825181
11 116755542 intron variant G/A snv 0.10
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2011 2011
dbSNP: rs12292921
rs12292921
11 116751247 intron variant T/G snv 0.10
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2009 2009
dbSNP: rs180327
rs180327
11 116752943 intron variant C/T snv 0.58
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs180327
rs180327
11 116752943 intron variant C/T snv 0.58
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs180327
rs180327
11 116752943 intron variant C/T snv 0.58
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs180327
rs180327
11 116752943 intron variant C/T snv 0.58
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2075295
rs2075295
11 116757685 intron variant T/C snv 0.31
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs28927680
rs28927680
11 116748357 3 prime UTR variant C/G;T snv
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs28927680
rs28927680
11 116748357 3 prime UTR variant C/G;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs3741300
rs3741300
11 116760974 intron variant G/A snv 0.36 0.34
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs3825041
rs3825041
11 116760991 intron variant T/A;C snv 0.89
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs4938310
rs4938310
11 116759233 intron variant C/T snv 0.19
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs6589564
rs6589564
11 116753437 intron variant C/A;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs6589565
rs6589565
11 116769521 intron variant A/G snv 0.93
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs6589565
rs6589565
11 116769521 intron variant A/G snv 0.93
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs6589565
rs6589565
11 116769521 intron variant A/G snv 0.93
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs6589565
rs6589565
11 116769521 intron variant A/G snv 0.93
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs7930786
rs7930786
11 116754011 intron variant C/G snv 0.92
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs11820589
rs11820589
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs11820589
rs11820589
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11820589
rs11820589
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012