Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35068180
MMP3
0.851 0.040 11 102845217 upstream gene variant A/-;AA delins 5
rs1537415
GLT6D1
0.851 0.040 9 135637876 intron variant G/C snv 0.36 4
rs12032672
PKN2-AS1
0.925 0.040 1 88159953 intron variant A/C snv 0.37 3
rs242016
CRACR2A
0.882 0.040 12 3679094 synonymous variant G/A snv 0.13 0.13 3
rs2521634
LOC107986777
0.882 0.040 7 24338421 intron variant G/A;C snv 3
rs3826782
ADGRE1
0.882 0.040 19 6887725 intron variant G/A snv 8.6E-02 3
rs7762544 0.882 0.040 6 41411577 intergenic variant G/A snv 0.81 3
rs1027009063
KIDINS220
0.925 0.040 2 8802974 stop gained G/A snv 2
rs1035029
C5
1.000 0.040 9 120980540 intron variant G/A snv 0.63 2
rs10760187 0.925 0.040 9 121803541 intergenic variant T/A;C snv 2
rs11084095
SIGLEC5
0.925 0.040 19 51623777 intron variant G/A snv 0.30 2
rs11621969 0.925 0.040 14 75347325 intergenic variant T/C snv 0.14 2
rs11800854 0.925 0.040 1 233584238 intergenic variant G/A snv 0.11 2
rs13145041 0.925 0.040 4 189616909 intergenic variant A/C;G;T snv 2
rs13237474 0.925 0.040 7 135816721 intron variant C/T snv 2.3E-02 2
rs1370967 0.925 0.040 5 111203694 intergenic variant G/A snv 7.8E-02 2
rs17879146
BIRC5
0.925 0.040 17 78223864 3 prime UTR variant T/G snv 1.2E-02 1.2E-02 2
rs1932040 0.925 0.040 6 45729051 TF binding site variant A/G snv 0.69 2
rs1953021 0.925 0.040 9 12914397 intergenic variant G/T snv 0.69 2
rs2569991
LOC105376956 ; LINC02022
0.925 0.040 3 12881698 intron variant C/A snv 0.72 2
rs2723183
IL37
1.000 0.040 2 112917144 missense variant A/G snv 6.8E-02 1.0E-01 2
rs4284742
SIGLEC5
0.925 0.040 19 51628480 intron variant A/G snv 0.78 2
rs6802315
MFSD1
0.925 0.040 3 158796571 intron variant T/A snv 0.59 2
rs6885116
TENM2
0.925 0.040 5 168216540 intron variant A/G snv 0.14 2
rs7086701 0.925 0.040 10 10298081 intergenic variant G/A;T snv 2