Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 8
rs3130618 0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 7
rs3132580 0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 7
rs9277534 0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38 7
rs3115663 0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 7
rs3130564 0.790 0.360 6 31133897 intron variant C/T snv 0.14 7
rs4958881 0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs7775397 0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 7
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 6
rs3130473 0.882 0.160 6 31231431 intergenic variant C/T snv 0.23 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs3132610 0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 6
rs558702 0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs1235162 0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs3132685 0.807 0.320 6 29978172 intron variant G/A;T snv 6
rs3131296 0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs11229 0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs7750641 0.807 0.360 6 31161533 missense variant C/T snv 7.0E-02 7.6E-02 6
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs2524005 0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 5
rs2233956 0.827 0.320 6 31113428 upstream gene variant T/C snv 0.12 5
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