Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 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
rs12711846
MIR4435-2HG ; ACOXL-AS1 ; ACOXL
0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26 4
rs2720680
PVT1
0.851 0.160 8 128102971 intron variant A/G snv 0.33 4
rs73005220
CIB3
0.851 0.160 19 16161878 intron variant A/G snv 3.9E-02 4
rs805294
LY6G6C ; MPIG6B
0.882 0.240 6 31720440 intron variant A/G snv 0.48 3
rs10881578
RXRA
0.925 0.240 9 134340689 intron variant A/G snv 0.32 2
rs3806624
EOMES
0.925 0.200 3 27723132 upstream gene variant A/G snv 0.61 2
rs4959089 0.925 0.200 6 32251948 upstream gene variant A/G snv 0.22 2
rs756440 0.925 0.160 6 33154554 intergenic variant A/G snv 0.24 2
rs7754200
LOC105375021 ; HLA-DPA3 ; HCG24
0.925 0.160 6 33143156 intron variant A/G snv 0.24 2
rs805286
LY6G6E ; LY6G6D ; LY6G6F-LY6G6D
1.000 0.120 6 31711530 intron variant A/G snv 0.42 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 13
rs11715604
NCK1
0.851 0.160 3 136870707 intron variant A/G;T snv 4
rs649775 0.882 0.120 6 33716536 upstream gene variant A/G;T snv 3
rs9267947 1.000 0.120 6 32243441 intergenic variant A/G;T snv 1
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs3093998 1.000 0.120 6 31517397 downstream gene variant C/A snv 0.70 1
rs35603048
BMF
0.851 0.160 15 40099764 intron variant C/A;G;T snv 4
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140