Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10148895 1.000 0.040 14 22254840 intron variant C/T snv 0.18 1
rs10441090 1.000 0.040 7 38295217 upstream gene variant C/T snv 0.13 1
rs10487742 1.000 0.040 7 38326911 non coding transcript exon variant G/A snv 0.14 1
rs11579261 1.000 0.040 1 143544453 intron variant T/A;C snv 1
rs11587304 1.000 0.040 1 143653074 upstream gene variant A/C snv 0.83 1
rs11975431 1.000 0.040 7 38322024 upstream gene variant C/T snv 0.14 1
rs11984094 1.000 0.040 7 38323965 upstream gene variant A/G snv 0.14 1
rs12154478 1.000 0.040 7 38290217 downstream gene variant G/A snv 6.9E-02 1
rs12881142 1.000 0.040 14 22268637 intron variant C/A;T snv 1
rs12888049 1.000 0.040 14 22026498 regulatory region variant G/A snv 0.30 1
rs17113407 1.000 0.040 14 22020341 intergenic variant T/C snv 6.7E-02 1
rs17161949 1.000 0.040 1 143550435 intron variant T/C snv 6.4E-02 1
rs17162082 1.000 0.040 1 143545399 intron variant C/T snv 5.0E-02 1
rs17171329 1.000 0.040 7 38316944 downstream gene variant C/T snv 7.3E-02 1
rs17171331 1.000 0.040 7 38323356 upstream gene variant T/C snv 1
rs17496969 1.000 0.040 7 38324688 upstream gene variant T/C snv 5.5E-02 1
rs1860517 1.000 0.040 7 38291209 downstream gene variant A/G snv 0.53 1
rs2027801 1.000 0.040 7 142712861 upstream gene variant G/A snv 0.48 1
rs2191312 1.000 0.040 7 38327658 intron variant C/T snv 0.26 1
rs2213212 1.000 0.040 7 142698925 downstream gene variant A/C snv 0.63 1
rs2240832 1.000 0.040 7 38289412 downstream gene variant T/C snv 0.27 1
rs2240839 1.000 0.040 7 38302324 upstream gene variant A/G snv 0.45 1
rs2240848 1.000 0.040 7 38321866 upstream gene variant A/G snv 5.5E-02 1
rs2240850 1.000 0.040 7 38324147 upstream gene variant C/A;G;T snv 1
rs2240851 1.000 0.040 7 38324328 upstream gene variant A/G;T snv 1