Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5574 | 0.882 | 0.200 | 7 | 24289514 | synonymous variant | C/T | snv | 0.43 | 0.43 | 5 | |
rs11178997 | 0.827 | 0.040 | 12 | 71938373 | upstream gene variant | T/A | snv | 0.12 | 5 | ||
rs9315202 | 0.925 | 0.080 | 13 | 33067879 | downstream gene variant | C/T | snv | 0.24 | 4 | ||
rs1876831 | 0.925 | 0.040 | 17 | 45830379 | non coding transcript exon variant | C/G;T | snv | 4.4E-06; 0.14 | 4 | ||
rs495225 | 0.882 | 0.040 | 3 | 172448243 | synonymous variant | G/A;C;T | snv | 0.66 | 4 | ||
rs9563121 | 0.925 | 0.080 | 13 | 33050369 | intron variant | C/T | snv | 0.26 | 4 | ||
rs4792887 | 0.882 | 0.080 | 17 | 45799654 | non coding transcript exon variant | C/T | snv | 0.16 | 4 | ||
rs386231 | 0.882 | 0.080 | 1 | 162356033 | intron variant | C/T | snv | 0.68 | 4 | ||
rs17759843 | 0.882 | 0.080 | 22 | 21920372 | 3 prime UTR variant | G/A | snv | 6.7E-02 | 4 | ||
rs4311 | 0.882 | 0.200 | 17 | 63483402 | intron variant | T/C | snv | 0.60 | 3 | ||
rs2400707 | 1.000 | 0.040 | 5 | 148825489 | 5 prime UTR variant | A/G;T | snv | 3 | |||
rs12944712 | 0.925 | 0.040 | 17 | 45793781 | intron variant | G/A | snv | 0.35 | 3 | ||
rs12364283 | 0.925 | 0.080 | 11 | 113476233 | upstream gene variant | A/G | snv | 5.8E-02 | 3 | ||
rs7552841 | 0.925 | 0.160 | 1 | 55053079 | intron variant | C/T | snv | 0.32 | 3 | ||
rs8042149 | 0.882 | 0.160 | 15 | 60832754 | intron variant | T/G | snv | 0.44 | 3 | ||
rs16965628 | 0.882 | 0.040 | 17 | 30228407 | intron variant | G/C | snv | 0.14 | 3 | ||
rs2267735 | 0.925 | 0.120 | 7 | 31095890 | intron variant | C/G | snv | 0.47 | 2 | ||
rs1042357 | 0.925 | 0.040 | 17 | 7001742 | synonymous variant | T/C;G | snv | 0.59 | 2 | ||
rs1799923 | 0.925 | 0.040 | 3 | 42264802 | 5 prime UTR variant | A/G | snv | 0.82 | 2 | ||
rs10055255 | 1.000 | 0.040 | 5 | 76968168 | intron variant | A/T | snv | 0.50 | 2 | ||
rs562010289 | 0.925 | 0.120 | 1 | 183227583 | missense variant | G/A;C | snv | 1.7E-04 | 2 | ||
rs6470292 | 1.000 | 0.040 | 8 | 124855801 | intron variant | A/G | snv | 0.17 | 2 | ||
rs683250 | 1.000 | 0.040 | 11 | 83565125 | intron variant | A/G;T | snv | 2 | |||
rs4775301 | 0.925 | 0.040 | 15 | 60834660 | intron variant | T/C;G | snv | 2 | |||
rs8024133 | 0.925 | 0.040 | 15 | 60838440 | intron variant | C/T | snv | 0.42 | 2 |