Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9856
XIAP
0.925 0.120 X 123911791 3 prime UTR variant C/T snv 0.57 4
rs9679162
GALNT14
0.882 0.120 2 31024648 intron variant G/T snv 0.48 4
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs9331888
CLU ; MIR6843
0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 5
rs931127
SIPA1 ; PCNX3
0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs9302752 0.925 0.120 16 50685192 upstream gene variant T/C snv 0.68 2
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs8371
XIAP
0.925 0.120 X 123912065 3 prime UTR variant C/T snv 0.25 0.19 4
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 12
rs8105637
TINCR
0.925 0.120 19 5566221 intron variant A/G snv 0.56 2
rs7963551
RAD52
0.807 0.160 12 912349 3 prime UTR variant T/G snv 0.13 7
rs781172058
CXCR4
0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs778962647
RUNX1T1
1.000 0.080 8 91986282 missense variant G/T snv 4.0E-06 1
rs778036161
RUNX1T1
0.776 0.080 8 92017363 missense variant T/C snv 8.0E-06 9
rs77382849
EIF3A
0.851 0.160 10 119050586 missense variant C/T snv 8.8E-03 4.4E-03 4
rs770327175
CXCR4
0.851 0.120 2 136115878 missense variant C/A;T snv 8.0E-06 5
rs767741751
MCPH1 ; ANGPT2
0.851 0.120 8 6562846 missense variant C/A snv 4.0E-06 5
rs766914563
LOC112268426 ; CXCR4
0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs763110
FASLG
0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs7628626
TIMMDC1 ; CD80
0.925 0.120 3 119525574 3 prime UTR variant A/C snv 0.82 2
rs761797378
MIR4273 ; LINC00960 ; ZNF717
1.000 0.080 3 75737671 missense variant T/A snv 2.0E-05 2.0E-05 1