Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3027012 1 159204333 5 prime UTR variant C/T snp 0.13 4
rs3741298 11 116786845 intron variant C/T snp 0.74 3
rs863002 1 159205130 intron variant C/T snp 0.29 3
rs998584 6 43790159 regulatory region variant C/A snp 0.41 3
rs11231693 11 64095140 intron variant G/A snp 0.12 2
rs1912826 4 186228386 intron variant G/A,C snp 0.57 2
rs6584202 10 98410626 non coding transcript exon variant G/A,C snp 0.37 2
rs987052 16 86288853 intron variant T/C snp 0.23 2
rs10039217 5 175751872 intergenic variant A/G snp 4.2E-02 1
rs10097849 8 14672342 intron variant T/G snp 0.54 1
rs10107366 8 98101459 T/C snp 1.7E-02 1
rs1011731 1 172377408 intron variant G/A snp 0.47 1
rs10131141 14 20793574 intergenic variant C/T snp 0.63 1
rs10198552 2 134842306 intron variant T/C snp 6.0E-02 1
rs1020410 2 175919410 intergenic variant T/C snp 0.33 1
rs10274047 7 134685727 intron variant T/G snp 0.33 1
rs1034207 6 127016554 intergenic variant C/T snp 0.93 1
rs10504576 8 74354444 intron variant A/G snp 0.47 1
rs1056513 1 61914626 missense variant G/A,C snp 0.57; 8.0E-06 0.50 1
rs10739496 9 97790277 intergenic variant C/G,T snp 0.72 1
rs10744816 12 114276461 regulatory region variant T/C snp 0.39 1
rs10818090 9 97799204 intergenic variant C/T snp 0.73 1
rs1084004 10 71362188 synonymous variant T/C,G snp 0.83 0.85 1
rs10894604 11 132771851 non coding transcript exon variant T/G snp 0.25 1
rs10983701 9 97775295 intergenic variant G/A snp 0.71 1