Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17424921 | 1.000 | 0.040 | 7 | 129068068 | upstream gene variant | G/C | snv | 0.11 | 1 | ||
rs2651804 | 1.000 | 0.040 | 11 | 2327389 | downstream gene variant | T/A;C | snv | 1 | |||
rs310746 | 1.000 | 0.040 | 3 | 12218116 | intergenic variant | C/T | snv | 0.93 | 1 | ||
rs4342938 | 1.000 | 0.040 | 10 | 131557214 | intergenic variant | A/G | snv | 0.41 | 1 | ||
rs4790797 | 1.000 | 0.040 | 17 | 5652037 | intergenic variant | G/A | snv | 0.44 | 1 | ||
rs6073976 | 1.000 | 0.040 | 20 | 45980011 | upstream gene variant | G/A | snv | 1 | |||
rs638376 | 1.000 | 0.040 | X | 114998678 | intergenic variant | T/C | snv | 0.54 | 1 | ||
rs685985 | 1.000 | 0.040 | 8 | 60652405 | intron variant | T/A;G | snv | 1 | |||
rs7130875 | 1.000 | 0.040 | 11 | 118742965 | intron variant | T/C | snv | 0.22 | 1 | ||
rs1035798 | 1.000 | 0.040 | 6 | 32183445 | splice region variant | G/A | snv | 0.24 | 0.19 | 1 | |
rs275652 | 1.000 | 0.040 | 3 | 148697197 | upstream gene variant | T/G | snv | 0.20 | 1 | ||
rs9884090 | 1.000 | 0.040 | 3 | 119397303 | intron variant | G/A | snv | 0.15 | 1 | ||
rs4134466 | 1.000 | 0.040 | 6 | 106129493 | intron variant | A/G | snv | 0.70 | 1 | ||
rs633724 | 1.000 | 0.040 | 6 | 106286165 | intron variant | C/T | snv | 0.42 | 1 | ||
rs661968 | 1.000 | 0.040 | 15 | 33968868 | 5 prime UTR variant | C/T | snv | 0.80 | 1 | ||
rs10946216 | 1.000 | 0.040 | 6 | 167125409 | intron variant | T/C | snv | 0.61 | 1 | ||
rs798036 | 1.000 | 0.040 | 1 | 116766208 | intron variant | T/A | snv | 0.17 | 1 | ||
rs10419538 | 1.000 | 0.040 | 19 | 35333116 | intron variant | C/G | snv | 0.11 | 1 | ||
rs10406069 | 1.000 | 0.040 | 19 | 35345627 | missense variant | G/A;C | snv | 0.16 | 1 | ||
rs10413500 | 1.000 | 0.040 | 19 | 35345923 | intron variant | C/G | snv | 0.16 | 1 | ||
rs11217020 | 1.000 | 0.040 | 11 | 118768644 | intron variant | G/A;C | snv | 1 | |||
rs11171747 | 1.000 | 0.040 | 12 | 56124624 | 3 prime UTR variant | T/A;G | snv | 1 | |||
rs753727908 | 1.000 | 0.040 | 1 | 161544759 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
rs4789182 | 1.000 | 0.040 | 17 | 75378864 | intron variant | G/A | snv | 0.55 | 1 | ||
rs883770 | 1.000 | 0.040 | 17 | 39907128 | non coding transcript exon variant | C/G;T | snv | 1 |