Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs145929329 | 0.882 | 0.040 | 9 | 22066213 | intron variant | TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTT | delins | 0.58 | 3 | ||
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 93 | |
rs3212227 | 0.566 | 0.840 | 5 | 159315942 | 3 prime UTR variant | T/G | snv | 0.26 | 65 | ||
rs78378222 | 0.662 | 0.360 | 17 | 7668434 | 3 prime UTR variant | T/G | snv | 8.3E-03 | 37 | ||
rs1273593548 | 0.716 | 0.160 | 7 | 106867593 | missense variant | T/G | snv | 8.4E-06 | 19 | ||
rs4295627 | 0.763 | 0.200 | 8 | 129673211 | intron variant | T/G | snv | 0.17 | 11 | ||
rs843720 | 0.752 | 0.280 | 2 | 54283523 | intron variant | T/G | snv | 0.52 | 10 | ||
rs7963551 | 0.807 | 0.160 | 12 | 912349 | 3 prime UTR variant | T/G | snv | 0.13 | 7 | ||
rs634537 | 0.851 | 0.080 | 9 | 22032153 | intron variant | T/G | snv | 0.28 | 6 | ||
rs11860248 | 0.882 | 0.040 | 16 | 24566445 | intron variant | T/G | snv | 0.27 | 5 | ||
rs891835 | 0.851 | 0.120 | 8 | 129479506 | intron variant | T/G | snv | 0.17 | 5 | ||
rs11337 | 0.925 | 0.120 | 8 | 41510767 | 3 prime UTR variant | T/G | snv | 0.93 | 4 | ||
rs13332653 | 0.882 | 0.040 | 16 | 24578078 | intergenic variant | T/G | snv | 0.11 | 3 | ||
rs2033214 | 0.882 | 0.040 | 16 | 24566199 | intron variant | T/G | snv | 0.14 | 3 | ||
rs12718945 | 1.000 | 0.040 | 7 | 55125270 | intron variant | T/G | snv | 0.51 | 1 | ||
rs17138945 | 1.000 | 0.040 | 7 | 116703812 | intron variant | T/G | snv | 7.3E-02 | 1 | ||
rs4253079 | 1.000 | 0.040 | 10 | 49514779 | intron variant | T/G | snv | 8.2E-02 | 1 | ||
rs1537375 | 0.882 | 0.120 | 9 | 22116072 | intron variant | T/C;G | snv | 6 | |||
rs944797 | 0.882 | 0.120 | 9 | 22115287 | intron variant | T/C;G | snv | 0.49 | 5 | ||
rs75061358 | 0.882 | 0.040 | 7 | 54848587 | intergenic variant | T/C;G | snv | 4 | |||
rs63751110 | 0.925 | 0.160 | 2 | 47410322 | missense variant | T/C;G | snv | 2 | |||
rs2065134 | 1.000 | 0.040 | 14 | 22788980 | intron variant | T/C;G | snv | 1 | |||
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 157 |