Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4879809 0.882 0.120 9 34635601 3 prime UTR variant T/A;C;G snv 1.1E-03; 1.00 3
rs695872 0.925 0.120 12 111599125 synonymous variant G/A snv 0.79 0.61 2
rs695871 1.000 0.080 12 111599196 missense variant G/C snv 0.77 0.61 2
rs2228576 0.851 0.160 12 6347896 missense variant T/A;C;G snv 4.5E-06; 0.69 4
rs3733242 1.000 0.080 4 76754352 missense variant C/A;T snv 2.4E-05; 0.46 1
rs11868035 0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 14
rs2303565 1.000 0.080 2 218680586 intron variant T/C snv 0.43 0.56 1
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs850713
GRN
1.000 0.080 17 44350364 intron variant G/A;T snv 0.28; 4.0E-06 1
rs2279238 0.790 0.320 11 47260473 missense variant C/T snv 0.26 0.26 11
rs10122902 1.000 0.080 9 27556782 synonymous variant G/A snv 0.24 0.21 1
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs2251644 1.000 0.080 14 102001510 intron variant A/G snv 0.17 0.21 1
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs11701 0.925 0.080 14 20693894 synonymous variant T/A;C;G snv 4.0E-06; 0.14 2
rs2529438 1.000 0.080 7 30595014 synonymous variant G/A;C snv 0.11 1
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs742710 0.925 0.080 20 5923382 missense variant C/T snv 0.11 0.12 2
rs11558538 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 19
rs1800435 0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 7
rs8141797 0.882 0.120 22 24186073 missense variant A/G snv 8.1E-02 9.8E-02 3
rs3806873 1.000 0.080 5 5462494 missense variant A/G snv 7.0E-02 3.4E-02 1