Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs72661131 0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs4711998 0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs555743307 0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51