Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
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
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 5
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10811650
CDKN2B-AS1
0.882 0.200 9 22067594 intron variant A/G snv 0.37 4
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 4
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs2725207
PKD2
0.882 0.200 4 88058377 intron variant C/A snv 0.31 3
rs3218020
CDKN2B-AS1
0.882 0.120 9 21997873 intron variant G/A;C snv 3
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 3
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 2
rs10995190
ZNF365
0.882 0.080 10 62518923 intron variant G/A snv 0.16 2
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 2
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 2