Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2516513
MICB-DT
0.925 0.120 6 31479811 downstream gene variant C/T snv 0.20 5
rs2734986
LOC105375010
0.827 0.160 6 29850791 intron variant T/C snv 0.10 5
rs2763979
HSPA1B
0.827 0.360 6 31826815 upstream gene variant C/T snv 0.45 5
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs707928
VWA7
0.827 0.320 6 31774813 intron variant A/G snv 0.47 5
rs1046089
PRRC2A
0.882 0.200 6 31635190 missense variant G/A snv 0.36 0.40 4
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs9392017 0.851 0.160 6 442357 intergenic variant G/A;C snv 4
rs649775 0.882 0.120 6 33716536 upstream gene variant A/G;T snv 3
rs805294
LY6G6C ; MPIG6B
0.882 0.240 6 31720440 intron variant A/G snv 0.48 3
rs13195441 0.925 0.200 6 32775521 intergenic variant G/A snv 0.30 2
rs181997 0.925 0.160 6 32932941 downstream gene variant G/A;C snv 2
rs2242660
PRRC2A
0.925 0.160 6 31629976 intron variant G/A snv 0.46 2
rs3129214 0.925 0.160 6 33149481 downstream gene variant C/T snv 0.24 2
rs3129223
HCG24 ; LOC105375021
0.925 0.160 6 33145420 intron variant C/T snv 0.24 2
rs3129234
HCG24 ; LOC105375021
0.925 0.160 6 33143570 upstream gene variant C/T snv 0.24 2
rs4959089 0.925 0.200 6 32251948 upstream gene variant A/G snv 0.22 2
rs6901221 0.925 0.160 6 33130499 downstream gene variant A/C snv 0.13 2
rs6928977
AHI1
0.925 0.120 6 135305210 intron variant T/G snv 0.70 2
rs756440 0.925 0.160 6 33154554 intergenic variant A/G snv 0.24 2
rs7745098
HBS1L
1.000 0.120 6 135093866 intron variant C/G;T snv 2
rs7754200
LOC105375021 ; HLA-DPA3 ; HCG24
0.925 0.160 6 33143156 intron variant A/G snv 0.24 2
rs1002658 1.000 0.120 6 137660447 intron variant C/T snv 0.15 1
rs2240064
CCHCR1
1.000 0.120 6 31146796 intron variant G/A;T snv 1
rs2523710
MICB-DT
1.000 0.120 6 31483132 intron variant G/A snv 0.14 1