Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5743708 | 0.525 | 0.800 | 4 | 153705165 | missense variant | G/A | snv | 1.7E-02 | 1.8E-02 | 98 | |
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 44 | ||
rs121917864 | 0.645 | 0.520 | 4 | 153704936 | missense variant | C/T | snv | 8.8E-05 | 9.8E-05 | 31 | |
rs2043211 | 0.653 | 0.480 | 19 | 48234449 | missense variant | A/T | snv | 0.33 | 0.29 | 29 | |
rs137854466 | 0.724 | 0.320 | 15 | 48411280 | stop gained | G/A;C | snv | 4.0E-05; 8.0E-06 | 23 | ||
rs727503054 | 0.732 | 0.200 | 15 | 48420752 | missense variant | A/G;T | snv | 1.6E-05 | 15 | ||
rs2118181 | 0.851 | 0.040 | 15 | 48623687 | intron variant | T/C | snv | 0.23 | 6 | ||
rs5516 | 0.827 | 0.120 | 19 | 50820217 | missense variant | C/G | snv | 0.69 | 0.67 | 6 | |
rs900 | 0.882 | 0.040 | 1 | 218441563 | 3 prime UTR variant | A/T | snv | 0.33 | 6 | ||
rs1036477 | 0.882 | 0.040 | 15 | 48622729 | intron variant | A/G | snv | 0.24 | 5 | ||
rs140598 | 0.827 | 0.160 | 15 | 48487333 | missense variant | G/A;C | snv | 3.2E-02 | 5 | ||
rs12191786 | 0.851 | 0.120 | 6 | 22004398 | intron variant | C/A;T | snv | 4 | |||
rs1465567 | 0.882 | 0.040 | 5 | 38370435 | missense variant | T/C | snv | 0.20 | 0.25 | 3 | |
rs4774517 | 0.882 | 0.040 | 15 | 48467094 | intron variant | G/T | snv | 0.34 | 3 | ||
rs10519177 | 0.925 | 0.040 | 15 | 48464998 | intron variant | A/G | snv | 0.35 | 2 | ||
rs755251 | 0.925 | 0.040 | 15 | 48519823 | intron variant | A/G;T | snv | 2 | |||
rs113358395 | 1.000 | 0.040 | 19 | 40714313 | missense variant | G/A;C | snv | 3.8E-03 | 3.5E-03 | 1 | |
rs191645600 | 1.000 | 0.040 | 9 | 136505728 | missense variant | G/T | snv | 5.8E-04 | 6.0E-04 | 1 | |
rs1343555503 | 1.000 | 0.040 | 18 | 51058364 | missense variant | G/A | snv | 4.0E-06 | 1 |