Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10039217 5 175751872 intergenic variant A/G snp 4.2E-02 1
rs10107366 8 98101459 T/C snp 1.7E-02 1
rs1020410 2 175919410 intergenic variant T/C snp 0.33 1
rs10274047 7 134685727 intron variant T/G snp 0.33 1
rs10744816 12 114276461 regulatory region variant T/C snp 0.39 1
rs11116045 12 83802750 intergenic variant A/G,T snp 0.28 1
rs11154370 6 126846446 intergenic variant A/G,T snp 3.2E-05; 2.6E-02 1
rs1128249 1.000 0.071 2 164672114 intron variant G/C,T snp 0.46 1
rs11715464 3 42868195 intron variant A/G snp 0.30 1
rs11754509 6 55608496 intergenic variant A/G snp 7.1E-02 1
rs11863065 16 82293200 intergenic variant G/A snp 6.7E-02 1
rs11974269 7 21108059 intergenic variant A/C snp 0.16 1
rs12023396 1 231134890 intergenic variant A/G snp 0.21 1
rs12195826 6 2565518 intergenic variant A/G snp 0.65 1
rs12586774 14 25660360 intergenic variant G/T snp 4.6E-02 1
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