Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10484554 0.807 0.200 6 31306778 intron variant C/T snv 0.12 8
rs2247056 0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs6457374 0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs2156875 0.882 0.200 6 31349570 intron variant C/T snv 0.50 6
rs6906846 0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 6
rs2894207 0.882 0.160 6 31295974 intron variant T/C snv 0.20 6
rs9366778 0.925 0.120 6 31301396 intron variant G/A snv 0.47 6
rs9264942 0.763 0.400 6 31306603 intron variant T/C snv 0.34 6
rs1058026 0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21 5
rs12191877 0.851 0.120 6 31285148 intron variant C/T snv 0.12 5
rs2523619 0.925 0.120 6 31350367 intron variant T/C snv 0.23 5
rs2844615 1.000 6 31275182 intron variant C/T snv 0.11 5
rs3819299 1.000 6 31354590 non coding transcript exon variant T/G snv 7.7E-02 2.3E-02 5
rs4386816 0.925 0.120 6 31279358 intron variant T/C snv 0.17 5
rs4394275 0.925 0.120 6 31350400 intron variant G/A snv 0.27 5
rs7382297 0.925 0.080 6 31279290 intron variant T/C;G snv 5
rs9265882 0.925 0.040 6 31345324 intron variant T/C snv 0.35 5
rs2249742 0.925 0.120 6 31272944 intron variant C/T snv 0.50 5
rs2395471 0.925 0.120 6 31272915 intron variant G/A snv 0.47 5
rs7759127 0.925 0.040 6 31273211 intron variant T/G snv 0.11 5
rs2524123 0.925 0.040 6 31297537 intron variant T/C snv 0.34 5
rs3873379 0.925 0.120 6 31294392 intron variant T/C snv 0.35 5
rs9380238 1.000 6 31299841 intron variant A/G snv 0.15 5
rs2523608 0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19 5
rs2394963 1.000 6 31283685 intron variant C/T snv 0.35 4