Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 4
rs10747083 12 132465032 downstream gene variant G/A;T snv 2
rs35859536 8 117179236 downstream gene variant C/T snv 0.25 2
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4
rs11558471 1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs3802177 1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 5
rs2292910 1.000 0.080 11 45882062 3 prime UTR variant A/C snv 0.66 3
rs3778321 6 7250037 3 prime UTR variant G/A snv 0.11 2
rs174550 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs11603334 1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 5
rs1552224 1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 4
rs2280231 11 47578886 5 prime UTR variant C/T snv 0.24 0.20 2
rs11715915
AMT
3 49417897 synonymous variant C/A;T snv 0.28 2
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs340874 0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs17762454 0.925 0.120 6 7212967 non coding transcript exon variant C/T snv 0.25 4
rs16980051 19 45842628 non coding transcript exon variant T/A;C snv 0.47 2
rs753993 11 47328418 non coding transcript exon variant C/A snv 0.33 2
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs2657879 1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 9
rs17265513 0.925 0.160 20 41203988 missense variant T/C snv 0.14 0.14 6
rs1124649 2 27037601 missense variant G/A snv 0.32 0.35 2
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 3
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22