Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2292779
AGO2
0.851 0.320 8 140551294 intron variant G/C;T snv 0.57; 4.9E-06 4
rs2425752
NCOA5
0.851 0.160 20 46073481 intron variant T/C snv 0.79 4
rs2546191
ELL2
0.851 0.160 5 95896837 intron variant G/A snv 0.38 4
rs2720680
PVT1
0.851 0.160 8 128102971 intron variant A/G snv 0.33 4
rs35603048
BMF
0.851 0.160 15 40099764 intron variant C/A;G;T snv 4
rs4525246
GRAMD1B
0.851 0.160 11 123524538 intron variant G/A;C snv 4
rs6546149
DTNB
0.851 0.160 2 25406569 intron variant C/G snv 0.38 4
rs6763508
ULK4
0.851 0.160 3 41709497 intron variant T/C snv 0.30 4
rs73005220
CIB3
0.851 0.160 19 16161878 intron variant A/G snv 3.9E-02 4
rs1860661
TCF3
0.882 0.120 19 1650135 intron variant A/C;G snv 6.7E-06; 0.54 3
rs3781093
GATA3
0.882 0.120 10 8059964 intron variant T/C snv 0.19 3
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
rs13255292
PVT1
0.925 0.120 8 128064327 intron variant C/T snv 0.24 2
rs2019960
PVT1
0.925 0.160 8 128180025 intron variant T/C snv 0.27 2
rs2242660
PRRC2A
0.925 0.160 6 31629976 intron variant G/A snv 0.46 2
rs3129223
HCG24 ; LOC105375021
0.925 0.160 6 33145420 intron variant C/T snv 0.24 2
rs34972832
CLEC16A
0.925 0.120 16 11105081 intron variant G/A;T snv 0.14 2
rs6928977
AHI1
0.925 0.120 6 135305210 intron variant T/G snv 0.70 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
rs1432295
LINC01185
1.000 0.120 2 60839531 intron variant G/A snv 0.69 1
rs2069757
TH2LCRR
1.000 0.120 5 132662721 intron variant G/A snv 7.5E-02 1
rs2240064
CCHCR1
1.000 0.120 6 31146796 intron variant G/A;T snv 1