Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 5
rs766432
BCL11A
0.925 0.080 2 60492835 intron variant C/A snv 0.80 5
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 4
rs6729815
BCL11A
1.000 0.080 2 60496537 intron variant T/C snv 0.49 4
rs7599488
BCL11A
0.925 0.120 2 60491212 intron variant C/T snv 0.42 4
rs7606173
BCL11A
1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 4
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 4
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 3
rs7565301
BCL11A
1.000 0.080 2 60496131 intron variant G/A snv 0.25 3
rs2541639
HBM
16 155036 intron variant G/A snv 0.21 3
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 3
rs11968814 1.000 0.080 6 71067268 intergenic variant G/A snv 4.4E-02 2
rs10172646
BCL11A
1.000 0.080 2 60493622 intron variant G/A snv 0.64 2
rs10195871
BCL11A
1.000 0.080 2 60493454 intron variant A/G;T snv 2
rs11886868
BCL11A
0.752 0.280 2 60493111 intron variant C/T snv 0.65 2
rs1427407
BCL11A
0.827 0.120 2 60490908 intron variant T/C;G snv 2
rs1896294
BCL11A
1.000 0.080 2 60491939 intron variant C/G;T snv 2
rs1896295
BCL11A
1.000 0.080 2 60496951 intron variant T/C snv 0.81 2
rs1896296
BCL11A
1.000 0.080 2 60496952 intron variant G/T snv 0.80 2
rs6545816
BCL11A
1.000 0.080 2 60487726 intron variant A/C;G snv 0.50 2
rs6545817
BCL11A
1.000 0.080 2 60488044 intron variant C/T snv 0.49 2
rs6706648
BCL11A
1.000 0.080 2 60494905 intron variant C/G;T snv 2
rs6738440
BCL11A
1.000 0.080 2 60495106 intron variant A/G snv 0.26 2
rs7557939
BCL11A
1.000 0.080 2 60494212 intron variant G/A snv 0.64 2