Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
rs3024505 | 0.790 | 0.320 | 1 | 206766559 | upstream gene variant | G/A | snv | 0.11 | 6 | ||
rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 6 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 3 | |
rs800292 | 0.645 | 0.560 | 1 | 196673103 | missense variant | G/A | snv | 0.32 | 0.40 | 3 | |
rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 2 | ||
rs2205960 | 0.763 | 0.400 | 1 | 173222336 | intergenic variant | G/A;T | snv | 2 | |||
rs3024493 | 0.776 | 0.280 | 1 | 206770623 | intron variant | C/A;T | snv | 0.11 | 2 | ||
rs4085613 | 0.827 | 0.160 | 1 | 152577542 | downstream gene variant | T/G | snv | 0.59 | 2 | ||
rs6677604 | 0.827 | 0.200 | 1 | 196717788 | intron variant | G/A | snv | 0.23 | 2 | ||
rs704840 | 0.851 | 0.240 | 1 | 173257056 | intergenic variant | T/G | snv | 0.29 | 2 | ||
rs7517847 | 0.689 | 0.600 | 1 | 67215986 | intron variant | T/G | snv | 0.37 | 2 | ||
rs1012507 | 1.000 | 0.080 | 1 | 173250332 | intergenic variant | G/T | snv | 0.32 | 1 | ||
rs10489265 | 0.827 | 0.200 | 1 | 173266926 | regulatory region variant | A/C | snv | 0.21 | 1 | ||
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 1 | |
rs10798269 | 1.000 | 0.080 | 1 | 173340574 | intergenic variant | A/G;T | snv | 1 | |||
rs10889681 | 0.925 | 0.160 | 1 | 67333487 | intron variant | T/A;C | snv | 1 | |||
rs10911628 | 1.000 | 0.080 | 1 | 184680369 | intergenic variant | C/A | snv | 9.4E-02 | 1 | ||
rs1130864 | 0.672 | 0.520 | 1 | 159713301 | 3 prime UTR variant | G/A | snv | 0.26 | 1 | ||
rs1205 | 0.602 | 0.680 | 1 | 159712443 | 3 prime UTR variant | C/T | snv | 0.30 | 1 | ||
rs12068671 | 0.925 | 0.160 | 1 | 172711891 | intergenic variant | T/C | snv | 0.23 | 1 | ||
rs1518111 | 0.790 | 0.360 | 1 | 206771300 | intron variant | T/C | snv | 0.71 | 1 | ||
rs16840639 | 0.925 | 0.120 | 1 | 196855643 | intron variant | T/C | snv | 0.23 | 1 | ||
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 1 |