Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1059449 1.000 0.120 6 29942921 missense variant G/A snv 6.1E-02 9.0E-02 1
rs1059536 1.000 0.080 6 29943448 missense variant A/C;G;T snv 4.1E-06; 0.17 3
rs1061235 6 29945521 3 prime UTR variant A/T snv 1
rs1061535 6 29970147 upstream gene variant T/C;G snv 1
rs1061539 1.000 0.040 6 29969778 downstream gene variant T/A;C snv 2
rs111312615 1.000 0.040 6 29955302 upstream gene variant T/G snv 2
rs1128306 0.925 0.120 6 29975492 non coding transcript exon variant G/A snv 0.22 2
rs113205291 1.000 0.040 6 29894844 upstream gene variant A/G;T snv 2
rs114204022 1.000 0.040 6 29972902 upstream gene variant G/A snv 2
rs114577328 1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02 2
rs114950038 1.000 0.040 6 29983056 downstream gene variant G/A;C snv 2
rs115559990 6 29926633 non coding transcript exon variant C/G;T snv 1
rs115625073 1.000 0.040 6 29924456 upstream gene variant T/C snv 2
rs115729734 1.000 0.080 6 29931238 upstream gene variant T/C;G snv 1
rs115928623 1.000 0.080 6 29971371 intron variant A/T snv 1
rs115960997 1.000 0.040 6 29934332 downstream gene variant G/A;T snv 2
rs12206499 1.000 0.040 6 29969350 downstream gene variant A/G snv 0.27 1
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs144304366 1.000 0.040 6 29936216 downstream gene variant T/C snv 2
rs147097402 1.000 0.080 6 29930083 upstream gene variant C/A;G;T snv 1
rs150881176 1.000 0.120 6 29979963 downstream gene variant T/C snv 1
rs1632879 6 29949926 downstream gene variant G/A snv 0.82 1
rs1632883 6 29948216 downstream gene variant C/A snv 0.78 1
rs1655900 1.000 0.080 6 29948841 downstream gene variant G/A snv 0.14 2
rs1655902 1.000 0.080 6 29949078 downstream gene variant G/A;C snv 1