Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35755165 | 0.882 | 0.080 | 19 | 40840084 | intron variant | A/C;G | snv | 5 | |||
rs4912913 | 0.827 | 0.120 | 5 | 143438741 | upstream gene variant | T/C | snv | 0.48 | 5 | ||
rs9295740 | 0.827 | 0.120 | 6 | 27721723 | intergenic variant | G/A | snv | 0.27 | 5 | ||
rs13191445 | 0.925 | 0.120 | 6 | 26015261 | upstream gene variant | G/A | snv | 5.6E-02 | 4 | ||
rs13212562 | 0.925 | 0.120 | 6 | 27332531 | intergenic variant | A/G | snv | 0.13 | 4 | ||
rs148696809 | 0.851 | 0.160 | 6 | 28966575 | downstream gene variant | T/C | snv | 5.3E-02 | 4 | ||
rs1862214 | 0.882 | 0.080 | 19 | 32544943 | intergenic variant | G/A;C | snv | 4 | |||
rs505974 | 0.882 | 0.080 | 3 | 190188984 | intergenic variant | T/C;G | snv | 4 | |||
rs568404 | 0.851 | 0.120 | 10 | 129233875 | regulatory region variant | C/A;G;T | snv | 4 | |||
rs7459185 | 0.851 | 0.160 | 7 | 76305323 | downstream gene variant | G/C;T | snv | 4 | |||
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 | ||
rs138488080 | 0.882 | 0.120 | 6 | 29638984 | upstream gene variant | G/A | snv | 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 |