Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs11932595 0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs738499 0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs1212171 0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 8
rs11824092 0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs10766075 0.925 0.080 11 13297040 intron variant C/T snv 0.27 6
rs11022778 0.925 0.080 11 13369313 intron variant T/A;G snv 6
rs156243 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 6
rs2291739 0.925 0.080 12 56420869 missense variant G/A;C snv 0.49; 4.0E-06 6
rs3789327 0.925 0.080 11 13363769 intron variant A/G snv 0.53 6