Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000005 21 33060745 intron variant G/C snp 0.51 2
rs10001106 4 10125817 intergenic variant T/A,C snp 0.37; 3.2E-05 1
rs1000113 0.923 0.036 5 150860514 intron variant C/T snp 0.13 2
rs10001632 4 10520247 intron variant A/C snp 0.98 1
rs10001964 4 9957651 intron variant C/T snp 0.47 1
rs10002082 4 164159753 intron variant A/G snp 0.18 1
rs10002268 1.000 0.071 4 55653725 intergenic variant T/C snp 0.41 1
rs1000291485 1.000 0.107 2 43844563 stop gained C/G snp 1
rs10002984 4 9679109 intergenic variant T/C snp 0.95 1
rs10003001 4 9982851 intron variant C/T snp 0.22 1
rs10003864 4 10435767 intergenic variant T/C snp 0.30 1
rs10004195 0.801 0.214 4 38783103 regulatory region variant T/A snp 0.27 7
rs10005067 4 87931491 intergenic variant T/A,C snp 0.40 1
rs10005684 4 9625273 intergenic variant T/A,G snp 0.89 1
rs1000579 1.000 0.071 4 4717767 intergenic variant A/G snp 0.44 1
rs1000592 1.000 0.036 2 118939624 intergenic variant C/A snp 6.2E-03 1
rs1000597 0.923 0.107 7 30897563 intron variant T/A,C snp 0.12 2
rs10006397 4 10034516 non coding transcript exon variant C/A snp 0.78 1
rs1000662 11 64466347 intergenic variant G/A snp 0.59 1
rs1000668 1.000 0.036 9 72790943 intron variant T/A,G snp 0.26 1
rs10007052 1.000 0.036 4 141084419 intron variant C/A snp 0.31 2
rs10007186 4 78667891 intron variant C/T snp 3.2E-05; 0.65 1
rs10007469 4 9731119 intergenic variant snp 0.90; 1.7E-02 1
rs10007754 4 103706285 intron variant T/G snp 0.32 1
rs1000778 11 61887833 intron variant A/G snp 0.61 2