Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs999885 0.925 0.120 7 100103553 intron variant G/A snv 0.56 0.46 3
rs10485138 1.000 0.080 6 100690714 intron variant C/T snv 2.5E-02 1
rs12649554 1.000 0.080 4 100975519 regulatory region variant T/C snv 0.65 1
rs3917267 0.882 0.080 2 102162359 intron variant G/A snv 0.32 3
rs17401966 0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs2185379 1.000 0.080 6 106088378 missense variant G/A snv 3.8E-02 4.5E-02 1
rs1010273 0.882 0.120 6 106107150 synonymous variant G/A snv 9.7E-02 7.7E-02 3
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs6937876 0.925 0.200 6 106132754 intron variant G/A snv 0.70 2
rs6568431 0.790 0.320 6 106140931 intron variant A/C snv 0.61 7
rs510432 0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs9514828 0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs12583006 0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs11569017
EGF
0.925 0.120 4 109980955 missense variant A/T snv 7.3E-02 5.0E-02 2
rs739496 0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 10
rs3782886 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs33932899 0.851 0.240 16 11254354 intron variant C/G;T snv 4
rs243327 0.882 0.280 16 11259447 intron variant A/G snv 0.52 4
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92