Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10508266 | 0.882 | 0.080 | 10 | 3797822 | intergenic variant | G/A;T | snv | 3 | |||
rs10512948 | 0.882 | 0.080 | 5 | 8233238 | intron variant | T/C | snv | 0.15 | 3 | ||
rs117781739 | 0.882 | 0.080 | 16 | 47835114 | intron variant | G/A;T | snv | 3 | |||
rs11878644 | 0.882 | 0.080 | 19 | 45373709 | upstream gene variant | T/C | snv | 0.53 | 3 | ||
rs13162612 | 0.882 | 0.080 | 5 | 8042908 | intergenic variant | A/G | snv | 5.1E-02 | 3 | ||
rs1560642 | 0.882 | 0.080 | 5 | 148888172 | intergenic variant | T/C;G | snv | 3 | |||
rs1663689 | 0.882 | 0.080 | 10 | 8983232 | intergenic variant | T/C | snv | 0.25 | 3 | ||
rs1814343 | 0.882 | 0.080 | 11 | 129695357 | regulatory region variant | C/T | snv | 0.22 | 3 | ||
rs2736107 | 0.882 | 0.080 | 5 | 1297739 | upstream gene variant | C/T | snv | 0.23 | 3 | ||
rs2924471 | 0.882 | 0.080 | 5 | 8055148 | intergenic variant | T/C | snv | 0.15 | 3 | ||
rs3742038 | 0.882 | 0.080 | 12 | 120371388 | non coding transcript exon variant | A/G | snv | 0.16 | 3 | ||
rs3856776 | 0.882 | 0.080 | 3 | 189580619 | intergenic variant | C/A;G;T | snv | 3 | |||
rs4665162 | 0.882 | 0.080 | 2 | 160203673 | intron variant | A/G | snv | 0.30 | 3 | ||
rs4785367 | 0.882 | 0.080 | 16 | 49922283 | non coding transcript exon variant | T/C | snv | 0.53 | 3 | ||
rs5756523 | 0.882 | 0.080 | 22 | 37117508 | intergenic variant | T/A;C | snv | 3 | |||
rs7248167 | 0.882 | 0.080 | 19 | 43455962 | downstream gene variant | A/C | snv | 0.22 | 3 | ||
rs7452888 | 0.882 | 0.080 | 6 | 169296169 | downstream gene variant | A/G | snv | 0.57 | 3 | ||
rs793544 | 0.882 | 0.080 | 3 | 107368152 | intron variant | T/C | snv | 0.35 | 3 | ||
rs7959801 | 0.882 | 0.080 | 12 | 120371787 | upstream gene variant | T/C | snv | 0.37 | 3 | ||
rs149518139 | 0.882 | 0.080 | 7 | 87566852 | missense variant | T/C | snv | 4.0E-06 | 3 | ||
rs2188524 | 0.882 | 0.080 | 7 | 87601119 | intron variant | T/C | snv | 3.2E-03 | 3 | ||
rs2235013 | 0.882 | 0.080 | 7 | 87549310 | intron variant | C/T | snv | 0.46 | 0.48 | 3 | |
rs7811989 | 0.882 | 0.080 | 7 | 17331739 | intron variant | A/G | snv | 0.76 | 3 | ||
rs1654701 | 0.882 | 0.080 | 8 | 107366717 | intron variant | G/A | snv | 0.52 | 3 | ||
rs4262299 | 0.882 | 0.080 | 8 | 107330035 | intron variant | A/C;T | snv | 3 |