Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1374313 2 119388079 regulatory region variant T/C snp 0.56 1
rs1443512 12 53948900 regulatory region variant A/C,T snp 0.67 1
rs1530530 13 24673148 intergenic variant A/G,T snp 4.2E-02 1
rs1624802 12 130012927 intergenic variant A/G,T snp 0.42; 2.0E-03 1
rs16933006 9 15335916 intergenic variant A/C snp 0.14 1
rs17064002 13 42996665 regulatory region variant C/T snp 1.7E-02 1
rs17102423 14 65138010 intergenic variant G/T snp 0.38 1
rs17668565 5 92818872 intergenic variant T/A,C snp 0.46 1
rs1776897 6 34227234 regulatory region variant G/T snp 0.81 1
rs2062550 16 85130995 regulatory region variant T/A,C snp 3.2E-05; 0.37 1
rs2820443 1.000 0.071 1 219580167 regulatory region variant T/C snp 0.23 1
rs2943636 2 226222568 intergenic variant G/A snp 0.44 1
rs3810541 20 57488263 intergenic variant C/T snp 0.30 1
rs430 7 19066916 intron variant G/A snp 4.8E-02 1
rs4749080 10 25873837 intergenic variant A/G snp 0.12 1
rs4810080 20 57483671 regulatory region variant A/G snp 0.36 1
rs4846567 1 219577375 intergenic variant G/T snp 0.22 1
rs6025590 20 57495449 regulatory region variant A/G snp 0.70 1
rs6099650 20 57483943 intergenic variant T/C snp 0.48 1
rs6099653 20 57487747 intergenic variant C/G snp 0.30 1
rs6834483 4 35981489 intron variant C/T snp 0.98 1
rs7355746 2 144594254 intergenic variant T/C snp 0.96 1
rs7612912 3 42869129 intron variant T/C snp 0.38 1
rs7645716 3 46295290 intergenic variant G/A snp 0.27 1
rs7654585 4 25941129 intergenic variant A/G snp 0.61 1