Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 5
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 4
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 4
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 3
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 3
rs11078903
CDK12
17 39475671 intron variant G/A;C;T snv 2
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 2
rs6066043
SLC13A3
1.000 0.080 20 46659814 intron variant G/A;T snv 2
rs10068737 5 118700852 intergenic variant T/A;C snv 1
rs12922822
UMOD
1.000 0.040 16 20356323 upstream gene variant C/A;T snv 1
rs1500896
C8orf37-AS1
8 95474454 intron variant G/A;C snv 1
rs174568
FADS1 ; FADS2
1.000 0.080 11 61826344 missense variant C/A;T snv 0.37 1
rs174580
FADS2
1.000 0.080 11 61839170 intron variant A/C;G snv 1
rs174581
FADS2
0.925 0.160 11 61839211 intron variant G/A;C snv 1
rs174594
FADS2
0.776 0.160 11 61852357 intron variant C/A;T snv 1
rs17577
SLC12A5-AS1 ; MMP9
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 1
rs2279463
SLC22A2
1.000 0.080 6 160247357 intron variant A/G;T snv 1
rs2887915 2 210689850 intergenic variant C/G;T snv 1
rs3093058
CRP
1 159715525 upstream gene variant T/A;C;G snv 1
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 1
rs4555246
DOK6
18 69609486 intron variant G/A;T snv 1