Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179 0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs13114738 0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs17249754 0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1869717 0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs2071410 0.882 0.160 15 90877710 intron variant C/A;G;T snv 7
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16