Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 57 | ||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 34 | |
rs1800961 | 0.851 | 0.160 | 20 | 44413724 | missense variant | C/T | snv | 3.1E-02 | 2.5E-02 | 21 | |
rs8192284 | 0.724 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 19 | |||
rs715 | 1.000 | 0.040 | 2 | 210678331 | 3 prime UTR variant | T/C | snv | 0.28 | 13 | ||
rs4129267 | 0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv | 13 | |||
rs7310615 | 0.882 | 12 | 111427245 | intron variant | C/G | snv | 0.67 | 12 | |||
rs4537545 | 0.790 | 0.160 | 1 | 154446403 | intron variant | C/T | snv | 0.48 | 11 | ||
rs6050 | 0.827 | 0.120 | 4 | 154586438 | missense variant | T/A;C | snv | 0.29 | 10 | ||
rs1800790 | 0.851 | 0.200 | 4 | 154562556 | upstream gene variant | G/A | snv | 0.15 | 9 | ||
rs12239046 | 1 | 247438293 | intron variant | T/C | snv | 0.58 | 9 | ||||
rs6734238 | 1.000 | 0.080 | 2 | 113083453 | upstream gene variant | A/G | snv | 0.39 | 8 | ||
rs10519203 | 0.851 | 0.080 | 15 | 78521704 | intron variant | G/A | snv | 0.67 | 8 | ||
rs7529229 | 0.851 | 0.120 | 1 | 154448302 | intron variant | T/C | snv | 0.48 | 8 | ||
rs1154988 | 3 | 136206349 | upstream gene variant | T/A | snv | 0.76 | 7 | ||||
rs1892534 | 0.925 | 0.120 | 1 | 65640261 | 3 prime UTR variant | C/T | snv | 0.44 | 7 | ||
rs4220 | 0.925 | 0.080 | 4 | 154570607 | missense variant | G/A | snv | 0.17 | 0.15 | 6 | |
rs6054 | 1.000 | 0.080 | 4 | 154568456 | missense variant | C/T | snv | 2.4E-03 | 2.7E-03 | 6 | |
rs12777 | 5 | 132335969 | synonymous variant | C/G | snv | 3.1E-02 | 2.8E-02 | 6 | |||
rs1539019 | 0.882 | 0.240 | 1 | 247436999 | intron variant | A/C | snv | 0.63 | 6 | ||
rs3091307 | 0.925 | 0.160 | 5 | 132653444 | intron variant | A/G | snv | 0.34 | 6 | ||
rs7681423 | 4 | 154621096 | intergenic variant | C/T | snv | 0.26 | 5 | ||||
rs7422339 | 1.000 | 0.080 | 2 | 210675783 | missense variant | C/A | snv | 5 | |||
rs2066861 | 4 | 154606284 | intron variant | C/T | snv | 0.26 | 5 |