Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10198241 | 0.925 | 0.080 | 2 | 226115660 | intergenic variant | T/C | snv | 0.58 | 4 | ||
rs10514299 | 0.827 | 0.120 | 5 | 88367793 | intron variant | C/T | snv | 0.21 | 6 | ||
rs110402 | 0.790 | 0.120 | 17 | 45802681 | intron variant | G/A;C | snv | 12 | |||
rs1137070 | 0.763 | 0.160 | X | 43744144 | synonymous variant | T/C | snv | 0.62 | 9 | ||
rs115357105 | 0.925 | 0.080 | 9 | 104376689 | intergenic variant | A/G | snv | 1.5E-02 | 4 | ||
rs11568817 | 0.790 | 0.120 | 6 | 77463665 | 5 prime UTR variant | A/C | snv | 0.37 | 8 | ||
rs1176744 | 0.708 | 0.240 | 11 | 113932306 | missense variant | A/C | snv | 0.33 | 0.36 | 19 | |
rs11825659 | 0.925 | 0.080 | 11 | 133925624 | intron variant | A/G | snv | 0.12 | 4 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs12180309 | 0.925 | 0.080 | 6 | 91209048 | intergenic variant | C/T | snv | 1.9E-02 | 4 | ||
rs12544026 | 0.925 | 0.080 | 8 | 101819970 | intron variant | G/A | snv | 0.85 | 4 | ||
rs12898460 | 0.882 | 0.080 | 15 | 38694612 | intron variant | C/T | snv | 0.23 | 3 | ||
rs12912251 | 0.882 | 0.080 | 15 | 38694167 | intron variant | G/T | snv | 0.25 | 3 | ||
rs130058 | 0.790 | 0.120 | 6 | 77463564 | 5 prime UTR variant | T/A;G | snv | 8 | |||
rs139438618 | 0.882 | 0.080 | 7 | 84008281 | intron variant | A/G | snv | 5.2E-02 | 5 | ||
rs1535255 | 0.807 | 0.120 | 6 | 88151489 | intron variant | T/G | snv | 0.21 | 8 | ||
rs16139 | 0.658 | 0.560 | 7 | 24285260 | missense variant | T/A;C | snv | 4.0E-06; 3.0E-02 | 36 | ||
rs173365 | 0.882 | 0.080 | 17 | 45823708 | intron variant | A/G | snv | 0.55 | 3 | ||
rs1800532 | 0.763 | 0.160 | 11 | 18026269 | intron variant | G/T | snv | 0.33 | 15 | ||
rs1824024 | 0.851 | 0.160 | 7 | 136958947 | intron variant | C/A | snv | 0.65 | 4 | ||
rs2061174 | 0.882 | 0.080 | 7 | 136976653 | intron variant | G/A;C | snv | 3 | |||
rs2094081 | 0.925 | 0.080 | 1 | 38927359 | intron variant | G/A;C | snv | 4 | |||
rs2273816 | 0.851 | 0.080 | 13 | 49719920 | intron variant | G/A;C | snv | 4 | |||
rs25531 | 0.581 | 0.520 | 17 | 30237328 | upstream gene variant | T/C | snv | 0.18 | 72 | ||
rs3219151 | 0.752 | 0.160 | 5 | 161701908 | 3 prime UTR variant | C/T | snv | 0.51 | 14 |