Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052486 0.851 0.200 6 31642909 missense variant A/G snv 0.51 0.44 4
rs3094127 0.925 0.200 6 30729670 intron variant A/G snv 0.27 3
rs3094694 0.925 0.200 6 30484127 upstream gene variant T/C snv 0.16 2
rs2746150 0.851 0.240 6 29474924 downstream gene variant C/T snv 5.3E-02 4
rs2844773 0.882 0.240 6 30239718 intron variant C/A snv 0.11 3
rs3094073 0.882 0.240 6 30263447 non coding transcript exon variant G/A snv 0.12 0.12 3
rs9262143 0.851 0.240 6 30685004 missense variant C/G;T snv 4.1E-06; 6.1E-02 4
rs1235162 0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs2517598 0.851 0.280 6 30112497 synonymous variant G/A snv 0.14 0.13 4
rs2523987 0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs2523989 0.827 0.280 6 30110498 missense variant C/T snv 0.12 0.12 5
rs2844659 0.851 0.280 6 30856755 intergenic variant C/G;T snv 4
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs3129791 0.827 0.280 6 28986516 intron variant G/A snv 5.3E-02 5
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs3130380 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs3132610 0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 6
rs9261290 0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2233956 0.827 0.320 6 31113428 upstream gene variant T/C snv 0.12 5
rs3132685 0.807 0.320 6 29978172 intron variant G/A;T snv 6
rs3134942 0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11 7
rs558702 0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16