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: rs1883025
rs1883025
0.807 0.120 9 104902020 intron variant C/T snv 0.28
High density lipoprotein measurement
0.800 1.000 10 2009 2019
dbSNP: rs12686004
rs12686004
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02
High density lipoprotein measurement
0.800 1.000 4 2011 2019
dbSNP: rs1883025
rs1883025
0.807 0.120 9 104902020 intron variant C/T snv 0.28
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2010 2018
dbSNP: rs3905000
rs3905000
0.925 0.080 9 104894789 intron variant G/A snv 0.14
High density lipoprotein measurement
0.800 1.000 4 2009 2019
dbSNP: rs2575876
rs2575876
9 104903458 intron variant G/A snv 0.24
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 3 2012 2018
dbSNP: rs2575876
rs2575876
9 104903458 intron variant G/A snv 0.24
High density lipoprotein measurement
0.800 1.000 3 2012 2019
dbSNP: rs3890182
rs3890182
0.925 0.120 9 104885374 intron variant G/A;T snv
High density lipoprotein measurement
0.800 1.000 3 2008 2019
dbSNP: rs9282541
rs9282541
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03
High density lipoprotein measurement
0.800 1.000 3 2008 2019
dbSNP: rs2515629
rs2515629
1.000 0.040 9 104832083 intron variant A/G snv 0.16
High density lipoprotein measurement
0.800 1.000 2 2011 2019
dbSNP: rs11789603
rs11789603
9 104884738 intron variant C/T snv 0.11
High density lipoprotein measurement
0.800 1.000 1 2012 2018
dbSNP: rs12686004
rs12686004
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2012 2018
dbSNP: rs1883025
rs1883025
0.807 0.120 9 104902020 intron variant C/T snv 0.28
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2012 2012
dbSNP: rs2575876
rs2575876
9 104903458 intron variant G/A snv 0.24
CUI: C0523744
Disease: Lipids measurement
Lipids measurement
0.800 1.000 1 2012 2012
dbSNP: rs4149268
rs4149268
1.000 0.040 9 104884939 intron variant C/T snv 0.46
High density lipoprotein measurement
0.800 1.000 1 2008 2008
dbSNP: rs2740488
rs2740488
0.827 0.120 9 104899461 intron variant A/C snv 0.29
High density lipoprotein measurement
0.700 1.000 5 2015 2019
dbSNP: rs2472386
rs2472386
1.000 0.040 9 104839260 intron variant G/A snv 0.47
High density lipoprotein measurement
0.700 1.000 3 2016 2019
dbSNP: rs1800978
rs1800978
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14
High density lipoprotein measurement
0.700 1.000 2 2018 2019
dbSNP: rs2740488
rs2740488
0.827 0.120 9 104899461 intron variant A/C snv 0.29
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2015 2018
dbSNP: rs2853579
rs2853579
9 104828991 synonymous variant G/T snv 0.20 0.23
High density lipoprotein measurement
0.700 1.000 2 2018 2019
dbSNP: rs3847302
rs3847302
9 104886314 intron variant A/G snv 0.12
High density lipoprotein measurement
0.700 1.000 2 2018 2019
dbSNP: rs7024300
rs7024300
9 104827286 intron variant C/T snv 5.8E-02
High density lipoprotein measurement
0.700 1.000 2 2016 2019
dbSNP: rs9282541
rs9282541
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs10820747
rs10820747
9 104924542 intron variant G/A snv 0.27
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs11789603
rs11789603
9 104884738 intron variant C/T snv 0.11
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs12686004
rs12686004
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018