Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2125685
FCGR2B
1.000 0.040 1 161673254 intron variant A/G;T snv 0.20 0.43 1
rs2392510
GPR141 ; EPDR1
1.000 0.040 7 37706967 intron variant C/T snv 0.47 1
rs9446777
KCNQ5
1.000 0.040 6 72871328 intron variant A/G snv 9.2E-02 1
rs2229092
LTA ; LOC100287329
1.000 0.040 6 31572980 missense variant A/C snv 4.7E-02 4.2E-02 1
rs10760187 0.925 0.040 9 121803541 intergenic variant T/A;C snv 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
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
rs2738058 0.925 0.160 8 6964095 upstream gene variant T/C snv 0.57 2
rs7086701 0.925 0.040 10 10298081 intergenic variant G/A;T snv 2
rs7567687 0.925 0.040 2 129276753 upstream gene variant C/T snv 0.43 2
rs9984417 0.925 0.040 21 22474790 intergenic variant A/T snv 0.52 2
rs17879146
BIRC5
0.925 0.040 17 78223864 3 prime UTR variant T/G snv 1.2E-02 1.2E-02 2
rs1035029
C5
1.000 0.040 9 120980540 intron variant G/A snv 0.63 2
rs2723183
IL37
1.000 0.040 2 112917144 missense variant A/G snv 6.8E-02 1.0E-01 2
rs1027009063
KIDINS220
0.925 0.040 2 8802974 stop gained G/A snv 2
rs1397780760
LOC105371777 ; KRT20
0.925 0.160 17 40884835 stop gained G/T snv 7.0E-06 2
rs733048
LOC105374494
0.925 0.040 4 13241173 intergenic variant G/A snv 0.21 2
rs2569991
LOC105376956 ; LINC02022
0.925 0.040 3 12881698 intron variant C/A snv 0.72 2
rs9979250
LOC400867
0.925 0.040 21 38911809 intron variant C/T snv 3.1E-02 2
rs6815464
MAEA
0.925 0.120 4 1316113 intron variant C/G;T snv 2