Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 24 | |||||
rs2472297 | 0.882 | 0.160 | 15 | 74735539 | intergenic variant | C/T | snv | 0.16 | 9 | ||
rs11642015 | 0.925 | 0.120 | 16 | 53768582 | intron variant | C/T | snv | 0.31 | 9 | ||
rs4410790 | 0.882 | 0.160 | 7 | 17244953 | intron variant | T/C | snv | 0.54 | 9 | ||
rs2567241 | 4 | 140402008 | missense variant | C/A | snv | 5.2E-02 | 6.0E-02 | 4 | |||
rs784257 | 1.000 | 0.080 | 18 | 55729968 | intron variant | T/A;C | snv | 4 | |||
rs838133 | 19 | 48756272 | synonymous variant | A/G;T | snv | 0.67; 4.0E-06 | 3 | ||||
rs7924036 | 10 | 63431885 | intron variant | G/A;T | snv | 3 | |||||
rs7072776 | 0.925 | 0.080 | 10 | 21744013 | downstream gene variant | A/G | snv | 0.65 | 3 | ||
rs33951980 | 7 | 73615107 | intron variant | C/T | snv | 0.10 | 3 | ||||
rs7619139 | 3 | 25068924 | intron variant | T/A | snv | 0.54 | 3 | ||||
rs34562254 | 1.000 | 0.160 | 17 | 16939677 | missense variant | G/A | snv | 0.14 | 0.12 | 3 | |
rs11104632 | 12 | 87829908 | intergenic variant | G/A | snv | 0.16 | 2 | ||||
rs8022678 | 14 | 98900353 | intergenic variant | A/C;G | snv | 2 | |||||
rs35397826 | 17 | 68273941 | missense variant | A/G | snv | 0.12 | 0.11 | 2 | |||
rs113918189 | 12 | 94325241 | intron variant | C/T | snv | 6.9E-02 | 2 | ||||
rs2984348 | X | 72308510 | intron variant | C/T | snv | 0.31 | 2 | ||||
rs148173957 | 1.000 | 0.040 | 5 | 56078195 | intron variant | TT/- | del | 8.2E-02 | 2 | ||
rs40465 | 1.000 | 0.040 | 5 | 104646025 | intron variant | T/G | snv | 0.24 | 2 | ||
rs7113624 | 11 | 87508051 | regulatory region variant | G/A;C | snv | 2 | |||||
rs643428 | 1 | 54263185 | intron variant | C/G;T | snv | 2 | |||||
rs7334078 | 13 | 98468230 | intron variant | T/C | snv | 0.29 | 2 | ||||
rs13211840 | 6 | 148791054 | intron variant | T/C | snv | 0.15 | 2 |