Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 13
rs2814778 0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 11
rs4148325 0.851 0.080 2 233764663 intron variant C/T snv 0.36 8
rs887829 0.763 0.280 2 233759924 intron variant C/T snv 0.36 8
rs2395029 0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 7
rs11157436 0.851 0.040 14 22168978 synonymous variant C/T snv 0.19 7
rs929596 0.925 0.040 2 233765830 intron variant A/G snv 0.32 7
rs17863787 0.925 0.040 2 233702448 intron variant T/G snv 0.30 7
rs13241427 1.000 7 1249003 regulatory region variant G/T snv 0.72 6
rs1329568 0.882 0.120 9 37037979 upstream gene variant T/A;G snv 6
rs143633948 0.882 0.080 6 131504454 intron variant G/A;C snv 6
rs73132848 0.882 0.080 3 8764738 intron variant G/A snv 9.3E-02 6
rs1015164 0.925 3 46410189 intron variant A/C;G;T snv 6
rs35897606 0.882 0.080 11 33436311 intron variant A/G snv 4.4E-02 6
rs79709413 0.882 0.080 13 24740488 upstream gene variant G/T snv 4.7E-02 6
rs73084982 0.882 0.080 20 3430406 intergenic variant G/A snv 3.5E-02 6
rs11790131 0.882 0.080 9 19469848 intergenic variant G/A;T snv 6
rs3815087 0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 6
rs35467001 0.882 0.080 17 73383923 missense variant G/A snv 5.3E-02 6.3E-02 6
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 6
rs10495970 1.000 2 49264671 intron variant G/A snv 0.26 5
rs11231017 0.925 11 62293877 downstream gene variant G/A snv 0.29 5
rs113974007 1.000 1 244750932 intergenic variant T/C snv 7.3E-02 5
rs11933652 1.000 4 28961215 intergenic variant T/C snv 0.12 5
rs13064773 0.925 3 158893105 intergenic variant G/A snv 0.39 5