Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 6
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 4
rs13211507
PGBD1
0.882 0.200 6 28289600 intron variant T/C snv 6.4E-02 4
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 4
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 4
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 4
rs9272219
HLA-DQA1
0.925 0.160 6 32634492 intron variant G/T snv 0.29 4
rs9467626
SLC17A3
0.882 0.160 6 25873518 intron variant C/A snv 7.3E-02 4
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 3
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 3
rs13199775
SLC17A1
0.882 0.160 6 25828554 intron variant A/T snv 7.4E-02 3
rs1892252
SLC17A4 ; SLC17A1
0.882 0.160 6 25772411 intron variant G/C snv 0.71 3
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 3
rs2070016
FGA
1.000 0.040 4 154589162 intron variant A/G snv 0.12 3
rs253
LPL
1.000 0.040 8 19953906 intron variant C/T snv 0.53 3
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 3
rs6939997
SLC17A1
0.882 0.160 6 25820996 intron variant C/T snv 7.0E-02 3