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: rs531819
rs531819
2 21040767 intron variant T/G snv 0.83
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs531819
rs531819
2 21040767 intron variant T/G snv 0.83
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs531819
rs531819
2 21040767 intron variant T/G snv 0.83
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs570877
rs570877
2 21028168 intron variant T/G snv 0.87
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs570877
rs570877
2 21028168 intron variant T/G snv 0.87
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs570877
rs570877
2 21028168 intron variant T/G snv 0.87
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12720826
rs12720826
2 21042823 intron variant T/C snv 3.8E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12720826
rs12720826
2 21042823 intron variant T/C snv 3.8E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12720826
rs12720826
2 21042823 intron variant T/C snv 3.8E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs1469513
rs1469513
1.000 0.080 2 21036690 intron variant T/C snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs533617
rs533617
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs533617
rs533617
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02
High density lipoprotein measurement
0.800 1.000 1 2012 2018
dbSNP: rs533617
rs533617
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2012 2018
dbSNP: rs533617
rs533617
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02
Low density lipoprotein cholesterol measurement
0.800 1.000 1 2012 2018
dbSNP: rs533617
rs533617
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2012 2018
dbSNP: rs533617
rs533617
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2854725
rs2854725
2 21014914 intron variant T/A;G snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2854725
rs2854725
2 21014914 intron variant T/A;G snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2854725
rs2854725
2 21014914 intron variant T/A;G snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10199768
rs10199768
2 21021128 intron variant G/T snv 0.35
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10199768
rs10199768
2 21021128 intron variant G/T snv 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs10199768
rs10199768
2 21021128 intron variant G/T snv 0.35
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs10199768
rs10199768
2 21021128 intron variant G/T snv 0.35
Low density lipoprotein cholesterol measurement
0.800 1.000 1 2011 2012
dbSNP: rs10199768
rs10199768
2 21021128 intron variant G/T snv 0.35
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs3791980
rs3791980
2 21022457 intron variant G/T snv 0.70
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012