Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs6815464
MAEA
0.925 0.120 4 1316113 intron variant C/G;T snv 2
rs6885116
TENM2
0.925 0.040 5 168216540 intron variant A/G snv 0.14 2
rs729876
SHISA9 ; LOC107984137
0.925 0.040 16 13294921 intron variant T/C snv 0.16 2
rs77490164
NKAIN2
0.925 0.040 6 124238586 intron variant C/T snv 4.4E-02 2
rs9979250
LOC400867
0.925 0.040 21 38911809 intron variant C/T snv 3.1E-02 2
rs9982623
MCM3AP
0.925 0.040 21 46271302 intron variant C/T snv 0.11 2
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
rs6681231 0.882 0.120 1 186690727 intergenic variant G/C snv 0.22 5
rs7762544 0.882 0.040 6 41411577 intergenic variant G/A snv 0.81 3
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
rs1370967 0.925 0.040 5 111203694 intergenic variant G/A snv 7.8E-02 2
rs1953021 0.925 0.040 9 12914397 intergenic variant G/T snv 0.69 2
rs7086701 0.925 0.040 10 10298081 intergenic variant G/A;T snv 2
rs733048
LOC105374494
0.925 0.040 4 13241173 intergenic variant G/A snv 0.21 2
rs9984417 0.925 0.040 21 22474790 intergenic variant A/T snv 0.52 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
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223