Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs744103
LOC105375069 ; LOC107986598
0.925 0.120 6 43837625 intron variant T/A snv 0.58 5
rs7442295
SLC2A9
0.925 0.120 4 9964756 intron variant A/G snv 0.28 5
rs7660895
SLC2A9
0.882 0.200 4 9983821 intron variant A/G;T snv 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs10011796
ABCG2
0.882 0.160 4 88169725 intron variant T/C;G snv 4
rs1028318
CARMIL1
0.925 0.120 6 25589996 intron variant T/C snv 0.27 4
rs10498730
SLC17A1
0.925 0.120 6 25811841 intron variant A/G snv 3.7E-02 4
rs10946785
CARMIL1
0.925 0.120 6 25616840 intron variant G/A;T snv 4
rs11066453
OAS1
1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 4
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
rs11264341
TRIM46
0.925 0.120 1 155179017 intron variant C/T snv 0.40 4
rs1165151
SLC17A1
0.925 0.120 6 25821388 intron variant T/A;G snv 4
rs1165152
SLC17A1
0.925 0.120 6 25818538 intron variant A/C;G;T snv 4
rs1165153
SLC17A1
0.925 0.120 6 25817561 intron variant A/G;T snv 4
rs1165160
SLC17A3
0.925 0.120 6 25864228 intron variant A/G snv 0.64 4
rs1165176
SLC17A1
0.925 0.120 6 25830070 intron variant A/G snv 0.65 4
rs1165177
SLC17A1
0.925 0.120 6 25829431 intron variant T/A snv 0.65 4
rs1165178
SLC17A1
0.925 0.120 6 25827288 intron variant A/G snv 0.65 4
rs1165182
SLC17A3
0.925 0.120 6 25837601 intron variant A/G snv 0.65 4
rs1165205
SLC17A3
0.925 0.120 6 25870314 intron variant T/A;G snv 4
rs1165207
SLC17A3
0.925 0.120 6 25865038 intron variant T/C snv 0.64 4
rs1165209
SLC17A1
0.925 0.120 6 25801091 intron variant G/A snv 0.66 4
rs1183200
SLC17A1
0.925 0.120 6 25818418 intron variant G/C snv 0.66 4
rs1183201
SLC17A1
0.925 0.120 6 25823216 intron variant A/T snv 0.65 4
rs1184803
SLC17A3
0.925 0.120 6 25834430 intron variant T/C snv 0.65 4