Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs116446171 0.851 0.160 6 484453 downstream gene variant C/G snv 2.3E-02 4
rs7765004 0.925 0.120 6 113750518 regulatory region variant A/C snv 0.32 2
rs79480871 0.925 0.160 2 24471603 intergenic variant C/T snv 9.3E-02 2
rs4733601 1.000 0.120 8 128257220 TF binding site variant A/G snv 0.41 1
rs6773363 1.000 0.120 3 27752141 intergenic variant T/A;C snv 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1164376164
ABCB1
0.851 0.200 7 87601024 5 prime UTR variant A/G snv 6
rs1390458638
ABCB6
0.925 0.120 2 219216441 missense variant G/A snv 4.0E-06 2
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs2231137
ABCG2
0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 13
rs41289586
ANO10
0.882 0.160 3 43577066 missense variant C/T snv 1.8E-02 1.9E-02 3
rs79464052
ARAP3
1.000 0.120 5 141655607 intron variant G/C snv 7.1E-02 7.8E-02 1
rs1312391542
ATG5 ; PRDM1
0.925 0.120 6 106104897 missense variant G/A;T snv 2
rs3218674
ATM
1.000 0.120 11 108244860 synonymous variant C/G;T snv 1.1E-02 1.1E-02 2
rs2279115
BCL2
0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv 18
rs1801018
BCL2
0.851 0.240 18 63318646 synonymous variant T/C snv 0.37 0.32 6
rs1880030
BCL7A
0.925 0.120 12 122046634 intron variant G/A snv 0.39 2
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24