Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs2618473 1.000 0.120 8 11486618 upstream gene variant C/T snv 0.34 1
rs4840565
BLK
1.000 0.120 8 11488036 intron variant G/C snv 0.33 1
rs1478900
BLK
1.000 0.120 8 11490151 intron variant C/G;T snv 1
rs1478901
BLK
1.000 0.120 8 11490324 intron variant G/C snv 0.25 1
rs9693589
BLK
1.000 0.120 8 11491452 intron variant G/A;C snv 1
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs2736343
BLK
1.000 0.120 8 11491741 intron variant C/T snv 0.83 1
rs2251056
BLK
1.000 0.120 8 11492067 intron variant C/A snv 0.83 1
rs2736344
BLK
1.000 0.120 8 11493169 intron variant T/C;G snv 1
rs9694294
BLK
1.000 0.120 8 11493212 intron variant C/G snv 0.82 1
rs4840568
BLK
0.882 0.160 8 11493510 intron variant G/A snv 0.32 4
rs1382568
BLK
0.925 0.160 8 11493711 intron variant A/C;G snv 2
rs922483
BLK
0.882 0.200 8 11494403 5 prime UTR variant C/T snv 0.31 3
rs2250788
BLK
1.000 0.120 8 11494547 5 prime UTR variant A/G;T snv 1
rs2736345
BLK
0.882 0.280 8 11494976 intron variant A/G snv 0.35 3
rs2618476
BLK
0.925 0.160 8 11495032 intron variant T/C snv 0.26 2
rs998683
BLK
1.000 0.120 8 11495491 intron variant G/A snv 0.25 1
rs998682
BLK
1.000 0.120 8 11495543 intron variant A/G snv 0.83 1
rs1478895
BLK
1.000 0.120 8 11495826 intron variant G/C snv 0.83 1
rs2618481
BLK
1.000 0.120 8 11496588 intron variant C/T snv 0.65 1
rs2250412
BLK
1.000 0.120 8 11497061 intron variant G/A;C snv 1
rs2618479
BLK
0.925 0.280 8 11498312 intron variant A/G snv 0.84 2
rs1478887
BLK
1.000 0.120 8 11498471 intron variant C/T snv 0.64 1