Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10741657 | 0.637 | 0.520 | 11 | 14893332 | upstream gene variant | A/G | snv | 0.65 | 34 | ||
rs2308321 | 0.653 | 0.480 | 10 | 129766800 | missense variant | A/G | snv | 9.3E-02 | 8.7E-02 | 29 | |
rs1223231582 | 0.677 | 0.280 | 7 | 142750639 | missense variant | A/G | snv | 7.0E-06 | 24 | ||
rs687289 | 1.000 | 0.120 | 9 | 133261703 | intron variant | A/G | snv | 15 | |||
rs746284240 | 0.763 | 0.240 | 12 | 68809243 | missense variant | A/G | snv | 11 | |||
rs1049074086 | 0.925 | 0.120 | 11 | 1759567 | missense variant | A/G | snv | 7.0E-06 | 9 | ||
rs11039149 | 0.827 | 0.280 | 11 | 47255124 | intron variant | A/G | snv | 0.19 | 6 | ||
rs281875322 | 0.807 | 0.480 | 18 | 51078306 | missense variant | A/G | snv | 4.0E-06 | 6 | ||
rs9564966 | 0.851 | 0.120 | 13 | 73322084 | intergenic variant | A/G | snv | 0.52 | 4 | ||
rs1209809979 | 0.925 | 0.120 | 1 | 45568989 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
rs4269383 | 0.882 | 0.120 | 6 | 155876368 | intergenic variant | A/G | snv | 0.37 | 3 | ||
rs4619 | 0.882 | 0.160 | 7 | 45893070 | missense variant | A/G | snv | 0.36 | 0.38 | 3 | |
rs11085754 | 0.925 | 0.120 | 19 | 11017920 | intron variant | A/G | snv | 0.41 | 2 | ||
rs12456874 | 0.925 | 0.120 | 18 | 13366863 | intron variant | A/G | snv | 0.20 | 2 | ||
rs1318 | 0.925 | 0.120 | 17 | 67695266 | 3 prime UTR variant | A/G | snv | 0.30 | 2 | ||
rs138147246 | 0.925 | 0.120 | 3 | 9756551 | synonymous variant | A/G | snv | 8.0E-06 | 1.4E-05 | 2 | |
rs1547374 | 0.925 | 0.120 | 21 | 42358786 | downstream gene variant | A/G | snv | 0.32 | 2 | ||
rs1810205 | 0.925 | 0.120 | 10 | 16923228 | intron variant | A/G | snv | 0.47 | 2 | ||
rs371609024 | 0.925 | 0.120 | 14 | 65629530 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
rs4149086 | 0.925 | 0.120 | 12 | 21239517 | 3 prime UTR variant | A/G | snv | 4.5E-04 | 2 | ||
rs4795218 | 0.925 | 0.120 | 17 | 37718512 | intron variant | A/G | snv | 0.82 | 2 | ||
rs5768709 | 0.925 | 0.120 | 22 | 48533757 | intron variant | A/G | snv | 0.36 | 2 | ||
rs708224 | 0.925 | 0.120 | 12 | 32283475 | intron variant | A/G | snv | 0.50 | 2 | ||
rs747601652 | 0.925 | 0.120 | 1 | 74723233 | missense variant | A/G | snv | 1.2E-05 | 2 | ||
rs935821839 | 0.925 | 0.120 | 1 | 3727199 | missense variant | A/G | snv | 7.0E-06 | 2 |