Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3829078
CA9
0.851 0.160 9 35679254 missense variant A/G;T snv 8.2E-02 6
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs4705341
CARMN
0.882 0.120 5 149426373 non coding transcript exon variant A/G snv 0.13 3
rs4784227
CASC16
0.807 0.160 16 52565276 intron variant C/T snv 0.20 8
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs14304
CCL18
1.000 0.080 17 36071135 3 prime UTR variant T/C snv 0.78 2
rs16893344
CCN4
0.807 0.160 8 133194036 intron variant C/T snv 0.29 7
rs3218038
CCNE1
0.882 0.120 19 29814988 intron variant G/T snv 9.1E-02 4
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs7186053
CDH1
1.000 0.080 16 68805390 intron variant A/G snv 0.69 1
rs438034
CENPF
0.882 0.120 1 214657274 stop gained A/G;T snv 0.61 4
rs738722
CHEK2
0.882 0.120 22 28734024 intron variant T/C snv 0.67 4
rs10399805
CHI3L1
0.851 0.240 1 203186870 upstream gene variant G/A;T snv 7
rs6691378
CHI3L1
0.882 0.160 1 203187994 upstream gene variant G/A snv 0.19 6
rs9331888
CLU ; MIR6843
0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 5
rs6720283
COL6A3
0.882 0.120 2 237401239 intron variant G/A snv 0.31 4
rs10420252
COX6B1
1.000 0.080 19 35648270 upstream gene variant G/A snv 9.7E-02 2
rs6510502
COX6B1
1.000 0.080 19 35647577 upstream gene variant A/C;G snv 2
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs781172058
CXCR4
0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs770327175
CXCR4
0.851 0.120 2 136115878 missense variant C/A;T snv 8.0E-06 5
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72