Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 8 | ||
rs9326246 | 0.925 | 0.040 | 11 | 116741017 | intergenic variant | C/G | snv | 0.93 | 8 | ||
rs2001844 | 0.882 | 0.040 | 8 | 125466503 | upstream gene variant | A/G | snv | 0.43 | 6 | ||
rs11014166 | 0.882 | 0.040 | 10 | 18419869 | intron variant | A/T | snv | 0.27 | 5 | ||
rs6544713 | 0.925 | 0.040 | 2 | 43846742 | non coding transcript exon variant | T/C | snv | 0.75 | 5 | ||
rs2144300 | 0.882 | 0.040 | 1 | 230159169 | intron variant | C/T | snv | 0.44 | 4 | ||
rs2301753 | 0.925 | 0.040 | 6 | 30071463 | missense variant | G/T | snv | 0.18 | 0.17 | 4 | |
rs611917 | 1.000 | 0.040 | 1 | 109272630 | non coding transcript exon variant | A/G | snv | 0.28 | 0.32 | 4 | |
rs13139571 | 1.000 | 0.040 | 4 | 155724361 | intron variant | C/A | snv | 0.22 | 3 | ||
rs16844401 | 1.000 | 0.040 | 4 | 3447925 | missense variant | G/A;T | snv | 7.5E-02; 8.3E-06 | 3 | ||
rs16948048 | 0.925 | 0.040 | 17 | 49363104 | intron variant | A/G | snv | 0.37 | 3 | ||
rs17608766 | 1.000 | 0.040 | 17 | 46935905 | 3 prime UTR variant | T/C | snv | 9.2E-02 | 3 | ||
rs1800787 | 1.000 | 0.040 | 4 | 154562863 | upstream gene variant | C/T | snv | 0.17 | 3 | ||
rs1800789 | 1.000 | 0.040 | 4 | 154561591 | upstream gene variant | G/A | snv | 0.17 | 3 | ||
rs2281719 | 1.000 | 0.040 | 1 | 230161913 | intron variant | C/T | snv | 0.45 | 3 | ||
rs247616 | 1.000 | 0.040 | 16 | 56955678 | intergenic variant | C/T | snv | 0.29 | 3 | ||
rs255052 | 0.925 | 0.040 | 16 | 67991092 | intron variant | G/A | snv | 0.17 | 0.17 | 3 | |
rs2681492 | 0.925 | 0.040 | 12 | 89619312 | intron variant | T/C;G | snv | 3 | |||
rs2865531 | 1.000 | 0.040 | 16 | 75356418 | intron variant | T/A | snv | 0.52 | 3 | ||
rs2967605 | 0.925 | 0.040 | 19 | 8404854 | downstream gene variant | C/T | snv | 0.20 | 3 | ||
rs2972146 | 0.882 | 0.040 | 2 | 226235982 | intergenic variant | G/T | snv | 0.72 | 3 | ||
rs507666 | 1.000 | 0.040 | 9 | 133273983 | intron variant | A/G | snv | 3 | |||
rs5167 | 1.000 | 0.040 | 19 | 44945208 | missense variant | T/A;G | snv | 3.6E-05; 0.39 | 3 | ||
rs585967 | 1.000 | 0.040 | 2 | 21047682 | upstream gene variant | A/C | snv | 0.81 | 3 | ||
rs715 | 1.000 | 0.040 | 2 | 210678331 | 3 prime UTR variant | T/C | snv | 0.28 | 3 |