Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10336 | 0.851 | 0.240 | 4 | 76001835 | 3 prime UTR variant | A/G;T | snv | 4 | |||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs1048412 | 1.000 | 6 | 30064718 | 3 prime UTR variant | A/G | snv | 0.15 | 0.17 | 1 | ||
rs10833 | 0.776 | 0.160 | 4 | 141733394 | 3 prime UTR variant | T/A;C | snv | 10 | |||
rs10892151 | 1.000 | 11 | 117661016 | intron variant | C/T | snv | 9.7E-02 | 3 | |||
rs11045819 | 0.851 | 0.120 | 12 | 21176879 | missense variant | C/A;T | snv | 0.11; 4.0E-06 | 4 | ||
rs1126477 | 0.807 | 0.200 | 3 | 46459778 | missense variant | C/T | snv | 0.34 | 0.53 | 7 | |
rs1126478 | 0.763 | 0.240 | 3 | 46459723 | missense variant | T/C | snv | 0.41 | 0.51 | 11 | |
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs11881222 | 0.925 | 0.080 | 19 | 39244283 | intron variant | A/G | snv | 0.30 | 3 | ||
rs1188975135 | 0.882 | 0.040 | 22 | 39017772 | missense variant | T/C | snv | 4.0E-06 | 4 | ||
rs1194919682 | 0.925 | 0.040 | 2 | 136115158 | missense variant | A/G | snv | 2 | |||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs12252 | 0.695 | 0.240 | 11 | 320772 | splice region variant | A/G | snv | 0.13 | 0.13 | 23 | |
rs1272938495 | 1.000 | 2 | 136115225 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | ||
rs1276738522 | 1.000 | 12 | 6232664 | start lost | A/G | snv | 4.9E-06 | 1 | |||
rs1292288729 | 1.000 | 19 | 41009375 | missense variant | T/C | snv | 7.4E-06 | 1 | |||
rs12979860 | 0.547 | 0.520 | 19 | 39248147 | intron variant | C/T | snv | 0.39 | 84 | ||
rs14158 | 0.851 | 0.160 | 19 | 11131368 | synonymous variant | G/A | snv | 0.24 | 0.22 | 5 | |
rs1433591886 | 1.000 | 2 | 169633213 | missense variant | G/A | snv | 4.0E-06 | 1 | |||
rs17235409 | 0.653 | 0.600 | 2 | 218395009 | missense variant | G/A;C | snv | 4.9E-02; 4.1E-06 | 31 | ||
rs1799864 | 0.572 | 0.680 | 3 | 46357717 | missense variant | G/A | snv | 0.13 | 0.12 | 68 | |
rs1799972 | 0.827 | 0.080 | 6 | 154039561 | missense variant | C/A;G;T | snv | 4.1E-06; 1.7E-02 | 6 | ||
rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 131 | |
rs1805192 | 0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv | 121 |