Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 8
rs2269426
TNXB
0.807 0.280 6 32108722 intron variant G/A snv 0.35 8
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs12663103
GPSM3
0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 7
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 7
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 7
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs9368699
SNHG32 ; SNORD48
0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 7
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 6
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 6