Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11152369 | 0.851 | 0.040 | 18 | 55399097 | intron variant | A/C | snv | 6.3E-02 | 5 | ||
rs1176744 | 0.708 | 0.240 | 11 | 113932306 | missense variant | A/C | snv | 0.33 | 0.36 | 19 | |
rs1333048 | 0.683 | 0.320 | 9 | 22125348 | intron variant | A/C | snv | 0.44 | 24 | ||
rs17673138 | 0.851 | 0.040 | 8 | 32840440 | intron variant | A/C | snv | 8.6E-02 | 4 | ||
rs7296288 | 0.851 | 0.080 | 12 | 49086185 | upstream gene variant | A/C | snv | 0.50 | 5 | ||
rs8321 | 0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 | 16 | |
rs12443954 | 0.851 | 0.040 | 16 | 89675088 | intron variant | A/C;G | snv | 5 | |||
rs878567 | 0.882 | 0.040 | 5 | 63960164 | intron variant | A/C;G | snv | 4 | |||
rs12487445 | 0.925 | 0.040 | 3 | 52584303 | intron variant | A/C;T | snv | 2 | |||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 21 | |||
rs1042779 | 0.882 | 0.040 | 3 | 52786995 | missense variant | A/G | snv | 0.40 | 0.42 | 4 | |
rs10748045 | 0.925 | 0.040 | 12 | 66422359 | intron variant | A/G | snv | 0.41 | 3 | ||
rs10968749 | 0.851 | 0.040 | 9 | 28752486 | intergenic variant | A/G | snv | 5.5E-02 | 4 | ||
rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 9 | ||
rs11773103 | 0.925 | 0.040 | 7 | 87192664 | non coding transcript exon variant | A/G | snv | 4.5E-02 | 2 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs12576775 | 0.827 | 0.080 | 11 | 79366149 | intron variant | A/G | snv | 0.15 | 6 | ||
rs140504 | 0.882 | 0.040 | 22 | 23285182 | missense variant | A/G | snv | 0.81 | 0.86 | 3 | |
rs16836940 | 0.925 | 0.040 | 1 | 150444437 | intron variant | A/G | snv | 0.31 | 2 | ||
rs17082664 | 0.925 | 0.040 | 6 | 152417619 | intron variant | A/G | snv | 0.17 | 2 | ||
rs17158930 | 0.851 | 0.040 | 7 | 111871082 | intron variant | A/G | snv | 0.25 | 4 | ||
rs17387100 | 0.925 | 0.040 | 4 | 15993502 | intron variant | A/G | snv | 7.5E-02 | 3 | ||
rs17662626 | 0.851 | 0.040 | 2 | 193119895 | intergenic variant | A/G | snv | 5.9E-02 | 5 | ||
rs1801260 | 0.695 | 0.280 | 4 | 55435202 | 3 prime UTR variant | A/G | snv | 0.25 | 28 | ||
rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 |