Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs7115242 0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs5065 0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs5063 0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs17568 0.752 0.320 1 1212042 synonymous variant C/T snv 0.37 0.31 12
rs765798193 0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs12369179 0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs7632505 0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs4714955 1.000 0.040 6 12903203 intron variant C/A;T snv 2
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs12190287 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs1869717 0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs1799998 0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14