Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs7681423 4 154621096 intergenic variant C/T snv 0.26 5
rs6050
FGA
0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 5
rs2066861
FGG
4 154606284 intron variant C/T snv 0.26 5
rs1800961 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 5
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs4129267 0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 4
rs4537545 0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs7518199 1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 4
rs7529229 0.851 0.120 1 154448302 intron variant T/C snv 0.48 4
rs7232 1.000 0.080 11 60173126 missense variant T/A snv 0.31 0.27 4
rs12239046 1 247438293 intron variant T/C snv 0.58 4
rs2073643 1.000 0.080 5 132387596 intron variant T/C snv 0.46 4
rs2158177 0.925 0.120 5 132648366 intron variant A/G snv 0.18 4
rs10034922 4 154599476 downstream gene variant G/A snv 5.2E-02 3
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 3
rs10226084 7 17957989 upstream gene variant T/C snv 0.46 3
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 3
rs12511469 4 154530607 downstream gene variant T/A snv 0.18 3
rs17690122 5 132532143 intron variant A/G;T snv 3
rs1938492 1 65652146 intergenic variant A/C snv 0.43 3
rs434943 14 68847342 intergenic variant G/A snv 0.27 3
rs4463047 4 154574381 downstream gene variant T/C snv 0.15 3