Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6857 | 0.790 | 0.240 | 19 | 44888997 | 3 prime UTR variant | C/T | snv | 0.13 | 8 | ||
rs9326246 | 0.925 | 0.040 | 11 | 116741017 | intergenic variant | C/G | snv | 0.93 | 8 | ||
rs9987289 | 1.000 | 0.040 | 8 | 9325848 | non coding transcript exon variant | A/G | snv | 0.87 | 8 | ||
rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 7 | |||
rs1122608 | 0.763 | 0.120 | 19 | 11052925 | intron variant | G/T | snv | 0.18 | 7 | ||
rs11902417 | 2 | 20976028 | intergenic variant | G/A | snv | 0.25 | 7 | ||||
rs17321515 | 0.776 | 0.200 | 8 | 125474167 | intron variant | A/G | snv | 0.49 | 7 | ||
rs2126259 | 1.000 | 8 | 9327636 | intron variant | T/C | snv | 0.87 | 7 | |||
rs2650000 | 0.851 | 0.200 | 12 | 120951159 | intron variant | A/C | snv | 0.70 | 7 | ||
rs2678379 | 1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 | 7 | ||
rs2954029 | 0.807 | 0.160 | 8 | 125478730 | intron variant | A/T | snv | 0.42 | 7 | ||
rs445925 | 0.882 | 0.080 | 19 | 44912383 | non coding transcript exon variant | G/A;C | snv | 7 | |||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 7 | |||
rs6589566 | 0.882 | 0.080 | 11 | 116781707 | intron variant | G/A;C;T | snv | 7 | |||
rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 7 | ||
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 6 | ||
rs10402271 | 1.000 | 0.080 | 19 | 44825957 | downstream gene variant | T/G | snv | 0.28 | 6 | ||
rs10455872 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 6 | ||
rs11568746 | 9 | 99105926 | intron variant | C/G | snv | 2.1E-05 | 6 | ||||
rs11571151 | 11 | 101127486 | missense variant | C/G;T | snv | 6 | |||||
rs11668477 | 0.925 | 0.080 | 19 | 11084354 | downstream gene variant | A/G | snv | 0.34 | 6 | ||
rs1874148 | 10 | 74114657 | intron variant | A/G | snv | 1.8E-02 | 6 | ||||
rs2001844 | 0.882 | 0.040 | 8 | 125466503 | upstream gene variant | A/G | snv | 0.43 | 6 | ||
rs2001945 | 8 | 125465736 | upstream gene variant | G/A;C;T | snv | 6 | |||||
rs2965101 | 1.000 | 0.080 | 19 | 44734556 | intergenic variant | T/C | snv | 0.34 | 6 |