Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12724990 1 100671474 intergenic variant G/A;C snv 1
rs221792
GIGYF1
7 100681034 3 prime UTR variant A/C;G;T snv 1
rs1754541
LOC101928334
1 101160327 intergenic variant A/G snv 0.25 2
rs7575217
TBC1D8
2 101160470 intron variant A/G snv 0.68 3
rs7168592
CHSY1
15 101183294 intron variant C/T snv 9.8E-02 4
rs111759324 1 101186966 upstream gene variant C/T snv 0.11 2
rs74431709 1 101187569 upstream gene variant T/G snv 0.11 1
rs12613485 2 101538302 intron variant G/A snv 8.9E-02 1
rs13062095 3 101548541 intergenic variant T/C snv 0.24 2
rs73177866 7 101728790 regulatory region variant A/T snv 0.37 1
rs115567723
MAP4K4
2 101746707 intron variant C/T snv 1.0E-02 1
rs111955202
MAP4K4
2 101788512 intron variant A/G snv 1.4E-02 1
rs114743735
IRAK2
3 10186296 intron variant C/G snv 4.2E-02 2
rs115820364
IRAK2
3 10187476 intron variant C/T snv 4.1E-02 1
rs6742301
LINC01127
2 101969429 intron variant C/T snv 0.32 1
rs150946191
IL1R1
2 102116028 intron variant T/G snv 1.9E-02 1
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs1997502
IL1RL2
2 102227789 intron variant A/G;T snv 1
rs56076326
CUX1
7 102237515 intron variant C/T snv 0.20 1
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 3
rs6543119
IL1RL1 ; IL18R1
2 102346612 intron variant A/T snv 0.36 1
rs5833013
IL1RL1 ; IL18R1
2 102352407 intron variant -/TA delins 2
rs9807989
IL18R1
1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 2
rs34020101
IL18RAP
2 102435015 non coding transcript exon variant AA/-;A;AAA delins 2
rs113473633
NFKB1
1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 4