Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs10801551 1.000 0.040 1 196610909 upstream gene variant G/A;C snv 2
rs10922144 1.000 0.040 1 196854170 intron variant C/A;T snv 2
rs10922146 1.000 0.040 1 196865506 intron variant C/T snv 0.19 2
rs12029571 1.000 0.040 1 196634172 intergenic variant A/G snv 0.24 2
rs12047098 1.000 0.040 1 196865976 intron variant T/C snv 0.19 2
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs1963605 1.000 0.040 1 196853038 intron variant C/A;T snv 2
rs1964645 1.000 0.040 1 196852884 intron variant T/A;C snv 2
rs4657825 1.000 0.040 1 196615191 intergenic variant A/G;T snv 2
rs6657442 1.000 0.040 1 196868930 intron variant T/C snv 0.19 2
rs7413265 1.000 0.040 1 196870033 intron variant G/T snv 0.19 2
rs7555070 1.000 0.040 1 197013024 downstream gene variant C/T snv 0.57 2
rs1021636 1.000 0.040 1 196876143 intron variant A/G snv 0.21 1
rs10510109 1.000 0.040 10 122360941 intergenic variant G/A;T snv 1
rs10754206 1.000 0.040 1 196851794 intron variant T/G snv 0.41 1
rs10801575 1.000 0.040 1 196883651 intron variant T/A;C snv 1
rs10887142 1.000 0.040 10 122347969 downstream gene variant G/A;C snv 1
rs11200576 1.000 0.040 10 122358034 intergenic variant A/T snv 0.13 1
rs11200583 1.000 0.040 10 122363954 regulatory region variant A/C snv 0.13 1
rs12240143 1.000 0.040 1 196875887 intron variant T/C snv 0.39 1
rs12240148 1.000 0.040 1 196876177 intron variant T/A;C snv 1
rs1332666 1.000 0.040 1 197015549 intergenic variant A/G;T snv 1
rs13374399 1.000 0.040 1 196872876 intron variant G/A snv 0.22 1