Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs652438 0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs3736228 0.752 0.400 11 68433827 missense variant C/T snv 0.13 0.11 13
rs2234694 0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02 3