Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 9
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 9
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 8
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 8
rs3749147
GPN1 ; CCDC121
0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 8
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 7
rs7691759 0.882 0.120 4 9686390 intron variant T/A;C snv 7
rs1178977
BAZ1B
0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21 7
rs7811265
BAZ1B
0.925 0.120 7 73520180 intron variant A/G snv 0.23 7
rs3817588
GCKR
0.882 0.160 2 27508345 intron variant T/C snv 0.14 7
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs3741414
INHBC
0.925 0.120 12 57450266 3 prime UTR variant C/T snv 0.19 7
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 7
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 7
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 7
rs1171614
SLC16A9
0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 7
rs683369
SLC22A1
0.807 0.360 6 160130172 missense variant G/A;C;T snv 4.0E-06; 0.83; 4.0E-06 7
rs16890979
SLC2A9
0.827 0.200 4 9920543 missense variant C/T snv 0.24 0.29 7
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 7
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 7
rs737267
SLC2A9
0.851 0.240 4 9933120 intron variant G/A;T snv 7