Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7634985 1.000 0.160 3 41978073 downstream gene variant C/T snv 0.72 1
rs78629637 1.000 0.160 3 41967289 intergenic variant C/A;T snv 1
rs794894 1.000 0.160 3 41990991 intergenic variant C/T snv 0.74 1
rs9835059 1.000 0.160 3 41968234 intergenic variant A/G;T snv 1
rs4148388 1.000 0.160 10 99790008 intron variant G/A;C snv 1
rs1450703683 1.000 0.160 X 8533018 missense variant T/C snv 1.9E-05 1
rs1250801605 1.000 0.160 2 201185809 missense variant G/A snv 4.0E-06 1
rs559979934 1.000 0.160 2 201185838 missense variant C/G;T snv 4.8E-05 2.1E-05 1
rs145738773 1.000 0.160 1 15504663 synonymous variant G/A snv 4.4E-05 1.0E-04 1
rs12158877 1.000 0.160 22 39153421 upstream gene variant T/G snv 0.45 1
rs139371 1.000 0.160 22 39123191 intron variant T/C;G snv 1
rs139385 1.000 0.160 22 39134127 non coding transcript exon variant C/A snv 0.46 1
rs139402 1.000 0.160 22 39150140 intron variant T/C snv 0.43 1
rs713841 1.000 0.160 22 39133024 3 prime UTR variant A/G snv 0.67 1
rs877529 1.000 0.160 22 39146287 intron variant G/A snv 0.43 1
rs3132535 1.000 0.160 6 31148749 intron variant A/G;T snv 0.69 1
rs11064392
CD4
1.000 0.160 12 6789226 intron variant A/G snv 0.14 1
rs12234262 1.000 0.160 7 21909685 intron variant C/T snv 0.49 1
rs12540021 1.000 0.160 7 21905945 intron variant G/A snv 0.22 1
rs4445125 1.000 0.160 7 21906222 intron variant C/T snv 0.42 1
rs4534048 1.000 0.160 7 21904567 intron variant A/G snv 0.24 1
rs56249828 1.000 0.160 7 21904989 intron variant T/C snv 0.25 1
rs6976370 1.000 0.160 7 21904621 intron variant A/G snv 0.40 1
rs1128226 1.000 0.160 7 21902051 3 prime UTR variant A/C snv 0.34 1
rs12700325 1.000 0.160 7 21901821 3 prime UTR variant A/G snv 0.20 1