Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs115689251 | 1.000 | 0.080 | 17 | 36032377 | intergenic variant | A/C | snv | 1.0E-02 | 2 | ||
rs6506900 | 1.000 | 0.080 | 18 | 31226433 | intergenic variant | A/C;G | snv | 2 | |||
rs7442201 | 1.000 | 0.080 | 4 | 4360022 | intron variant | A/C;G | snv | 2 | |||
rs6754498 | 1.000 | 0.080 | 2 | 185953121 | non coding transcript exon variant | A/C;G;T | snv | 2 | |||
rs10738610 | 0.882 | 0.120 | 9 | 22123767 | intron variant | A/C;T | snv | 5 | |||
rs10757274 | 0.701 | 0.320 | 9 | 22096056 | intron variant | A/G | snv | 0.41 | 22 | ||
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 44 | ||
rs114031744 | 1.000 | 0.080 | 10 | 123610085 | intergenic variant | A/G | snv | 1.7E-02 | 2 | ||
rs13175840 | 1.000 | 0.080 | 5 | 133861647 | regulatory region variant | A/G | snv | 0.25 | 2 | ||
rs1412829 | 0.742 | 0.400 | 9 | 22043927 | intron variant | A/G | snv | 0.28 | 14 | ||
rs2383206 | 0.742 | 0.320 | 9 | 22115027 | intron variant | A/G | snv | 0.49 | 17 | ||
rs2383207 | 0.695 | 0.280 | 9 | 22115960 | intron variant | A/G | snv | 0.64 | 22 | ||
rs2891168 | 0.851 | 0.160 | 9 | 22098620 | intron variant | A/G | snv | 0.40 | 5 | ||
rs4272321 | 1.000 | 0.080 | 7 | 158159143 | intron variant | A/G | snv | 4.6E-04 | 2 | ||
rs76294234 | 1.000 | 0.080 | 4 | 83241025 | intron variant | A/G | snv | 1.5E-02 | 2 | ||
rs7689240 | 1.000 | 0.080 | 4 | 35313869 | intergenic variant | A/G | snv | 0.21 | 2 | ||
rs9641609 | 1.000 | 0.080 | 7 | 118657790 | regulatory region variant | A/G | snv | 0.38 | 2 | ||
rs2680830 | 1.000 | 0.080 | 2 | 17596817 | intron variant | A/G;T | snv | 0.94 | 2 | ||
rs4977574 | 0.695 | 0.520 | 9 | 22098575 | intron variant | A/G;T | snv | 26 | |||
rs543554 | 1.000 | 0.080 | 13 | 32127501 | intron variant | A/G;T | snv | 2 | |||
rs77934287 | 1.000 | 0.080 | 12 | 23071319 | intron variant | A/G;T | snv | 2 | |||
rs1481805 | 1.000 | 0.080 | 8 | 71121190 | intron variant | A/T | snv | 0.58 | 2 | ||
rs59811240 | 1.000 | 0.080 | 8 | 124709787 | intron variant | C/A | snv | 1.3E-02 | 2 | ||
rs117854110 | 1.000 | 0.080 | 7 | 105603002 | upstream gene variant | C/A;T | snv | 2 | |||
rs6606859 | 1.000 | 0.080 | 15 | 27032254 | intron variant | C/A;T | snv | 2 |