Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9913156
ARRB2
17 4721671 downstream gene variant C/G;T snv 1
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 2
rs9895848
MINK1
17 4835663 intron variant C/T snv 0.25 1
rs9658111
PPARD
6 35396757 intron variant G/C snv 0.15 1
rs9494142
LOC105378010
6 135110502 TF binding site variant T/C snv 0.21 3
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 3
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 4
rs9272219
HLA-DQA1
0.925 0.160 6 32634492 intron variant G/T snv 0.29 1
rs9263737 6 31141768 upstream gene variant G/A;C snv 1
rs8141529
ZNRF3
22 28873704 intergenic variant A/G snv 0.33 1
rs79716587
ARHGAP15
2 143129250 intron variant G/A snv 7.9E-02 3
rs79478560
DNAH10
12 123914608 intron variant G/A snv 0.36 0.41 1
rs7939778 11 100636316 intergenic variant G/A;C snv 1
rs79237520
MACROH2A1
5 135376876 intron variant C/T snv 1.6E-02 1
rs7901056 10 26423554 regulatory region variant T/G snv 0.44 1
rs77372977 1 101267901 downstream gene variant C/G;T snv 1
rs77216612
LOC107984129 ; APOLD1 ; LOC105369663
12 12725049 upstream gene variant A/G snv 0.20 1
rs77046277 1 101279090 intergenic variant C/G snv 1.2E-03 1
rs7650602
ZBTB38
1.000 0.040 3 141428572 intron variant T/C snv 0.51 2
rs76382185 1 101182070 regulatory region variant C/T snv 8.0E-02 1
rs7578575
DNMT3A
2 25265950 intron variant T/A snv 0.27 2
rs7576541
ACOXL
2 110849824 intron variant C/A;G;T snv 1
rs748113
VSIR ; CDH23
10 71749034 3 prime UTR variant T/C snv 0.38 3
rs73579370
LINC00565
13 113930357 upstream gene variant T/A;C;G snv 1
rs73243398
LINC01258
4 38450959 intron variant G/A;C snv 9.8E-02 1