Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13111638
SLC2A9 ; LOC105374476
0.882 0.200 4 9995266 intron variant T/C snv 0.82 4
rs10783124 1.000 0.080 1 99937719 intergenic variant A/G snv 2.9E-02 1
rs7583877
AFF3
0.925 0.080 2 99844192 intron variant C/T snv 0.61 2
rs7562121
AFF3
1.000 0.080 2 99767892 intron variant C/G snv 0.66 1
rs59834205
SLC2A9
0.882 0.200 4 9959396 intron variant -/GA delins 1.1E-04 3
rs149454410
SLC2A9
0.925 0.120 4 9942000 missense variant C/G;T snv 4.0E-05; 3.2E-04 5
rs161740
CHD1
0.882 0.200 5 98869326 intron variant C/A;T snv 3
rs2236242
SERPINA12
0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs17709344
LOC107983974
0.925 0.080 15 93608310 intron variant G/A snv 4.0E-02 2
rs12437854
LOC107983974
0.925 0.080 15 93598604 intron variant T/G snv 0.10 2
rs594442 1.000 0.080 6 93138166 intergenic variant A/C;T snv 1
rs553908921
CCSER1
1.000 0.080 4 91329657 intron variant C/T snv 1.4E-05 1
rs62416056
GJA10
1.000 0.080 6 89918054 intron variant G/C snv 0.13 2
rs148240484
DPEP1
1.000 0.080 16 89637333 missense variant G/A;C;T snv 5.3E-04; 3.9E-04; 4.0E-06 3
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 5
rs1049255
CYBA
0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 9
rs2576178
RNLS ; LIPJ
0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs4148155
ABCG2
0.882 0.200 4 88133515 intron variant A/G snv 8.7E-02 5
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1372834938
KIDINS220
0.763 0.280 2 8812465 missense variant G/C snv 4.2E-06 12
rs2229109
ABCB1
0.807 0.240 7 87550493 missense variant C/A;T snv 2.7E-02 8
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs147084429
LINC02188
1.000 0.080 16 86727784 intron variant C/T snv 1.4E-02 1
rs80282103
LARP4B
1.000 0.080 10 853131 intron variant A/T snv 0.12 4