Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17424921 1.000 0.040 7 129068068 upstream gene variant G/C snv 0.11 1
rs2651804 1.000 0.040 11 2327389 downstream gene variant T/A;C snv 1
rs310746 1.000 0.040 3 12218116 intergenic variant C/T snv 0.93 1
rs4342938 1.000 0.040 10 131557214 intergenic variant A/G snv 0.41 1
rs4790797 1.000 0.040 17 5652037 intergenic variant G/A snv 0.44 1
rs6073976 1.000 0.040 20 45980011 upstream gene variant G/A snv 1
rs638376 1.000 0.040 X 114998678 intergenic variant T/C snv 0.54 1
rs685985 1.000 0.040 8 60652405 intron variant T/A;G snv 1
rs7130875 1.000 0.040 11 118742965 intron variant T/C snv 0.22 1
rs1035798
AGER
1.000 0.040 6 32183445 splice region variant G/A snv 0.24 0.19 1
rs275652
AGTR1
1.000 0.040 3 148697197 upstream gene variant T/G snv 0.20 1
rs9884090
ARHGAP31
1.000 0.040 3 119397303 intron variant G/A snv 0.15 1
rs4134466
ATG5
1.000 0.040 6 106129493 intron variant A/G snv 0.70 1
rs633724
ATG5
1.000 0.040 6 106286165 intron variant C/T snv 0.42 1
rs661968
AVEN ; CHRM5
1.000 0.040 15 33968868 5 prime UTR variant C/T snv 0.80 1
rs10946216
CCR6
1.000 0.040 6 167125409 intron variant T/C snv 0.61 1
rs798036
CD2
1.000 0.040 1 116766208 intron variant T/A snv 0.17 1
rs10419538
CD22
1.000 0.040 19 35333116 intron variant C/G snv 0.11 1
rs10406069
CD22 ; MIR5196
1.000 0.040 19 35345627 missense variant G/A;C snv 0.16 1
rs10413500
CD22 ; MIR5196
1.000 0.040 19 35345923 intron variant C/G snv 0.16 1
rs11217020
DDX6
1.000 0.040 11 118768644 intron variant G/A;C snv 1
rs11171747
ESYT1 ; ZC3H10
1.000 0.040 12 56124624 3 prime UTR variant T/A;G snv 1
rs753727908
FCGR3A
1.000 0.040 1 161544759 missense variant C/G;T snv 4.0E-06; 8.0E-06 1
rs4789182
GRB2
1.000 0.040 17 75378864 intron variant G/A snv 0.55 1
rs883770
GSDMB
1.000 0.040 17 39907128 non coding transcript exon variant C/G;T snv 1