Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs987763 6 126960402 intron variant C/A;T snv 1
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs2229616 0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 2
rs7797307 7 69221140 intron variant G/C snv 7.6E-02 1
rs12731740 1 207851475 intron variant C/T snv 9.1E-02 1
rs6931262 6 7217284 non coding transcript exon variant C/T snv 0.10 1
rs2278426 1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 2
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs2235529 1.000 0.040 1 22123994 intron variant C/T snv 0.13 1
rs2277339 12 56752285 missense variant T/G snv 0.12 0.14 1
rs1876829 1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14 2
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs1051921 0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs17249754 0.882 0.120 12 89666809 intron variant G/A snv 0.15 3
rs1055144 1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs55747707 7 73623036 intron variant G/A snv 0.16 1
rs2287019 1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 2
rs987237 0.925 0.120 6 50835337 intron variant A/G snv 0.17 3
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs3088050 5 177299634 3 prime UTR variant G/A snv 0.18 1
rs8070723 0.851 0.240 17 46003698 intron variant A/G snv 0.18 5
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs9750952 1.000 0.080 2 238827723 intergenic variant C/T snv 0.19 1
rs12714415 2 651430 intergenic variant T/C snv 0.19 2