Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 9
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 7
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 6
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 6
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29 6
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 5
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5