Source: ALL
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 13
rs11886868
BCL11A
0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 11
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 10
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 10
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 9
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 6
rs1427407
BCL11A
0.827 0.120 2 60490908 intron variant T/C;G snv 6
rs766432
BCL11A
0.925 0.080 2 60492835 intron variant C/A snv 0.80 6
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
rs7606173
BCL11A
1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 5
rs1547247
HBS1L
6 135069698 intron variant G/A snv 0.22 5
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
rs7482144
HBG2
0.882 0.280 11 5254939 3 prime UTR variant G/A snv 4
rs2541639
HBM
16 155036 intron variant G/A snv 0.21 4
rs13027161
MIR4432HG
2 60380593 intron variant T/C snv 0.29 4
rs2137283
MIR4432HG
2 60385322 non coding transcript exon variant C/A snv 0.30 4
rs10445937 2 60410521 intron variant G/A snv 0.39 3
rs12464462 2 60409281 intron variant A/G;T snv 0.39 3
rs12476132 2 60412769 intron variant G/A snv 0.34 3
rs13009393 2 60406229 intron variant G/A snv 0.33 3
rs243063 2 60395764 intron variant A/T snv 0.35 3
rs243066 2 60394631 intron variant A/G snv 0.29 3