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 | 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 |