Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs221798 | 0.882 | 0.040 | 7 | 100689872 | intron variant | C/A;G | snv | 3 | |||
rs221774 | 0.851 | 0.080 | 7 | 100701361 | upstream gene variant | A/G;T | snv | 4 | |||
rs506597 | 0.882 | 0.040 | 7 | 100715797 | upstream gene variant | A/G | snv | 0.90 | 4 | ||
rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 5 | ||
rs7914558 | 0.851 | 0.040 | 10 | 103016151 | intron variant | G/A | snv | 0.40 | 5 | ||
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 12 | ||
rs6484218 | 0.882 | 0.040 | 11 | 10369034 | intron variant | G/A | snv | 0.21 | 4 | ||
rs7337127 | 0.925 | 0.080 | 13 | 104623579 | intergenic variant | C/A;T | snv | 2 | |||
rs12669727 | 1.000 | 0.040 | 7 | 104776829 | intron variant | T/A;C | snv | 1 | |||
rs735931 | 1.000 | 0.040 | 3 | 10483412 | intron variant | A/G | snv | 0.60 | 1 | ||
rs9297357 | 0.851 | 0.040 | 8 | 105130105 | intron variant | C/G;T | snv | 5 | |||
rs73188321 | 1.000 | 0.040 | 7 | 105407711 | intergenic variant | C/T | snv | 0.35 | 1 | ||
rs6738485 | 0.882 | 0.040 | 2 | 106193504 | intron variant | C/T | snv | 0.36 | 3 | ||
rs111940429 | 0.925 | 0.080 | 2 | 107366232 | intron variant | C/A;T | snv | 2 | |||
rs12871532 | 0.851 | 0.040 | 13 | 108016199 | intergenic variant | T/C | snv | 0.46 | 5 | ||
rs3804640 | 1.000 | 0.040 | 3 | 108074862 | intron variant | A/G | snv | 0.39 | 1 | ||
rs17040430 | 1.000 | 0.040 | 12 | 108349043 | regulatory region variant | G/T | snv | 5.9E-02 | 1 | ||
rs1536057 | 1.000 | 0.040 | 6 | 108564420 | intron variant | C/T | snv | 0.30 | 1 | ||
rs56031956 | 0.882 | 0.040 | 9 | 108863349 | missense variant | C/G | snv | 2.3E-02 | 2.2E-02 | 3 | |
rs7959663 | 0.925 | 0.040 | 12 | 109446562 | intron variant | G/A;C | snv | 2 | |||
rs10884920 | 1.000 | 0.040 | 10 | 110015049 | intron variant | A/G;T | snv | 1 | |||
rs121912734 | 0.925 | 0.120 | 12 | 110339638 | missense variant | T/C | snv | 1 | |||
rs12833856 | 1.000 | 0.040 | 12 | 110824378 | intergenic variant | A/G | snv | 1.6E-02 | 1 | ||
rs6568686 | 1.000 | 0.040 | 6 | 111551279 | intron variant | T/C | snv | 0.83 | 1 | ||
rs77867520 | 0.882 | 0.040 | 4 | 11186225 | intergenic variant | C/T | snv | 7.2E-02 | 3 |