Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10468017 | 0.851 | 0.120 | 15 | 58386313 | intron variant | C/T | snv | 0.24 | 10 | ||
rs10503669 | 0.925 | 0.080 | 8 | 19990179 | intergenic variant | C/A | snv | 8.4E-02 | 7 | ||
rs12678919 | 0.882 | 0.080 | 8 | 19986711 | intergenic variant | A/G | snv | 1.0E-01 | 7 | ||
rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 8 | ||
rs1532085 | 0.882 | 0.080 | 15 | 58391167 | intron variant | A/G;T | snv | 9 | |||
rs1532624 | 0.851 | 0.160 | 16 | 56971567 | intron variant | C/A | snv | 0.34 | 7 | ||
rs157580 | 0.882 | 0.160 | 19 | 44892009 | intron variant | G/A | snv | 0.69 | 11 | ||
rs17321515 | 0.776 | 0.200 | 8 | 125474167 | intron variant | A/G | snv | 0.49 | 7 | ||
rs173539 | 0.882 | 0.080 | 16 | 56954132 | intergenic variant | C/T | snv | 0.33 | 7 | ||
rs174546 | 0.807 | 0.200 | 11 | 61802358 | 3 prime UTR variant | C/T | snv | 0.28 | 9 | ||
rs174547 | 0.742 | 0.240 | 11 | 61803311 | intron variant | T/C | snv | 0.28 | 10 | ||
rs174570 | 0.882 | 0.200 | 11 | 61829740 | intron variant | C/T | snv | 0.15 | 10 | ||
rs1864163 | 0.882 | 0.120 | 16 | 56963321 | intron variant | G/A | snv | 0.26 | 8 | ||
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 7 | ||
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 12 | ||
rs2083637 | 0.925 | 0.080 | 8 | 20007664 | intergenic variant | A/G | snv | 0.25 | 6 | ||
rs2144300 | 0.882 | 0.040 | 1 | 230159169 | intron variant | C/T | snv | 0.44 | 4 | ||
rs2156552 | 1.000 | 0.040 | 18 | 49655298 | downstream gene variant | A/G;T | snv | 4 | |||
rs2271293 | 1.000 | 0.040 | 16 | 67868167 | intron variant | G/A | snv | 0.11 | 3 | ||
rs2338104 | 1.000 | 0.040 | 12 | 109457363 | non coding transcript exon variant | C/G | snv | 0.58 | 3 | ||
rs2515629 | 1.000 | 0.040 | 9 | 104832083 | intron variant | A/G | snv | 0.16 | 3 | ||
rs255049 | 1.000 | 0.040 | 16 | 67979568 | intron variant | T/C | snv | 0.34 | 3 | ||
rs2943634 | 0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv | 4 | |||
rs2967605 | 0.925 | 0.040 | 19 | 8404854 | downstream gene variant | C/T | snv | 0.20 | 3 | ||
rs3764261 | 0.732 | 0.280 | 16 | 56959412 | upstream gene variant | C/A | snv | 0.31 | 11 |