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
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 127
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 117
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 91
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 86
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 75
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17