Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4721295 | 0.882 | 0.040 | 7 | 1997034 | intron variant | T/G | snv | 0.33 | 3 | ||
rs10275045 | 0.882 | 0.160 | 7 | 1881190 | intron variant | C/T | snv | 0.35 | 2 | ||
rs59574136 | 1.000 | 0.040 | 7 | 1996825 | intron variant | T/C | snv | 0.10 | 2 | ||
rs140364877 | 1.000 | 0.040 | 7 | 1845542 | non coding transcript exon variant | C/T | snv | 4.3E-03 | 2 | ||
rs58120505 | 1.000 | 0.040 | 7 | 1990232 | intron variant | T/C | snv | 0.37 | 2 | ||
rs12699477 | 1.000 | 0.120 | 7 | 1929317 | intron variant | T/C | snv | 0.28 | 2 | ||
rs3823624 | 1.000 | 0.040 | 7 | 2070711 | intron variant | T/C | snv | 0.17 | 2 | ||
rs11514731 | 1.000 | 0.040 | 7 | 2011868 | intron variant | C/G | snv | 0.16 | 2 | ||
rs4236274 | 1.000 | 0.040 | 7 | 1856777 | intron variant | A/G | snv | 0.47 | 1 | ||
rs3931398 | 1.000 | 0.040 | 7 | 1991957 | intron variant | G/A | snv | 1 | |||
rs4332037 | 1.000 | 0.040 | 7 | 1911173 | intron variant | C/T | snv | 0.19 | 1 | ||
rs117829095 | 7 | 1892738 | intron variant | C/A;T | snv | 1 | |||||
rs11770148 | 7 | 1859811 | intron variant | A/G;T | snv | 1 | |||||
rs4721096 | 1.000 | 0.040 | 7 | 1837675 | intron variant | T/C | snv | 0.84 | 1 | ||
rs4721135 | 7 | 1872586 | intron variant | A/G | snv | 0.37 | 1 | ||||
rs12666575 | 1.000 | 0.040 | 7 | 1964786 | intron variant | C/G;T | snv | 1 | |||
rs12668848 | 1.000 | 0.040 | 7 | 1981360 | intron variant | G/A;T | snv | 1 | |||
rs6461049 | 1.000 | 0.040 | 7 | 1977810 | intron variant | C/T | snv | 0.56 | 1 | ||
rs13234909 | 7 | 1827295 | intron variant | G/A | snv | 0.33 | 1 | ||||
rs57633152 | 7 | 2002912 | intron variant | C/G | snv | 0.46 | 1 | ||||
rs10950456 | 1.000 | 0.040 | 7 | 1940114 | 5 prime UTR variant | G/A | snv | 0.57 | 1 | ||
rs11763750 | 7 | 2040479 | intron variant | G/A | snv | 0.16 | 1 | ||||
rs34731055 | 7 | 2067293 | intron variant | C/T | snv | 0.13 | 1 | ||||
rs13240401 | 7 | 2154761 | intron variant | T/A;C | snv | 1 | |||||
rs34782622 | 7 | 2155497 | intron variant | A/G | snv | 0.14 | 1 |