Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7194
HLA-DRA
0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 5
rs3129878
HLA-DRA
0.807 0.360 6 32440958 intron variant A/C snv 0.30 2
rs498422
TSBP1 ; TSBP1-AS1
0.882 0.160 6 32318984 intron variant T/G snv 0.14 2
rs10248566 1.000 0.040 7 91638848 non coding transcript exon variant G/C snv 0.25 1
rs11937871 1.000 0.040 4 103871299 upstream gene variant C/T snv 0.27 1
rs12097821 0.882 0.040 1 106793679 regulatory region variant G/A;T snv 1
rs12429186 1.000 0.040 13 33718141 regulatory region variant T/C snv 2.7E-02 1
rs2501443 1.000 0.040 7 122902383 intergenic variant A/G snv 0.47 1
rs253296 1.000 0.040 5 150573187 intergenic variant G/A snv 0.28 1
rs312620 1.000 0.040 5 143980913 intergenic variant T/A snv 4.2E-02 1
rs4959523 1.000 0.040 6 1193180 intergenic variant A/G snv 0.12 1
rs6546680 1.000 0.040 2 71236304 regulatory region variant C/G;T snv 1
rs7023221 1.000 0.040 9 16085264 intergenic variant T/C snv 0.48 1
rs7192993 1.000 0.040 16 7961213 intron variant A/G snv 0.29 1
rs7523497 1.000 0.040 1 62387475 regulatory region variant A/G snv 0.79 1
rs7802723 1.000 0.040 7 138244561 intergenic variant T/A;C snv 1
rs821693 1.000 0.040 10 106360432 intergenic variant A/G;T snv 0.87 1
rs967004 1.000 0.040 4 141923771 intergenic variant G/A snv 0.73 1
rs9958292 1.000 0.040 18 7303203 upstream gene variant G/T snv 0.33 1
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 1
rs2076531
BTNL2 ; TSBP1-AS1
1.000 0.040 6 32395935 intron variant A/G;T snv 1
rs7166401
CHSY1
1.000 0.040 15 101235913 intron variant A/G snv 0.32 1
rs12614
CYP21A2 ; CFB
0.851 0.160 6 31946402 missense variant C/G;T snv 4.1E-06; 0.12 1
rs7317862
FAM155A
1.000 0.040 13 107253690 intron variant A/C snv 0.11 1
rs2584345
FAT1
1.000 0.040 4 186606664 intron variant T/C snv 0.46 1