Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7697932 | 1.000 | 0.120 | 4 | 100084161 | intron variant | A/G | snv | 0.72 | 1 | ||
rs779805 | 0.851 | 0.120 | 3 | 10141653 | 5 prime UTR variant | G/A;C | snv | 4 | |||
rs776399733 | 0.882 | 0.120 | 3 | 10141965 | missense variant | C/A;T | snv | 6.5E-06 | 3 | ||
rs869025621 | 0.882 | 0.240 | 3 | 10142079 | missense variant | A/C;G;T | snv | 4 | |||
rs5030805 | 0.790 | 0.280 | 3 | 10142086 | missense variant | G/A;T | snv | 7 | |||
rs104893829 | 0.882 | 0.240 | 3 | 10142088 | missense variant | C/T | snv | 2.0E-04 | 3.8E-04 | 4 | |
rs5030807 | 0.851 | 0.320 | 3 | 10142113 | missense variant | T/A;C | snv | 5 | |||
rs5030809 | 0.776 | 0.320 | 3 | 10142139 | missense variant | T/C | snv | 1.3E-05 | 10 | ||
rs104893824 | 0.776 | 0.320 | 3 | 10142181 | missense variant | T/A;C | snv | 8 | |||
rs1064794272 | 0.807 | 0.240 | 3 | 10146566 | missense variant | C/A | snv | 6 | |||
rs121913346 | 0.925 | 0.240 | 3 | 10149796 | missense variant | T/A;C | snv | 3 | |||
rs5030818 | 0.882 | 0.280 | 3 | 10149804 | stop gained | C/G;T | snv | 4 | |||
rs5030820 | 0.827 | 0.280 | 3 | 10149822 | missense variant | C/G;T | snv | 8.0E-06 | 6 | ||
rs5030823 | 0.851 | 0.280 | 3 | 10149871 | stop gained | C/A;G;T | snv | 4.0E-06 | 4 | ||
rs5030824 | 0.776 | 0.320 | 3 | 10149885 | missense variant | C/G | snv | 2.0E-05 | 4.2E-05 | 9 | |
rs869025668 | 0.882 | 0.240 | 3 | 10149964 | stop lost | G/T | snv | 3 | |||
rs5742714 | 0.882 | 0.160 | 12 | 102396074 | 3 prime UTR variant | C/G | snv | 8.9E-02 | 3 | ||
rs28362491 | 0.592 | 0.720 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 56 | |||
rs9420907 | 0.790 | 0.320 | 10 | 103916707 | intron variant | C/A;G | snv | 7 | |||
rs11813268 | 0.925 | 0.120 | 10 | 103922538 | upstream gene variant | C/T | snv | 0.31 | 2 | ||
rs2297235 | 0.752 | 0.320 | 10 | 104274733 | 5 prime UTR variant | A/G | snv | 0.22 | 11 | ||
rs156697 | 0.672 | 0.560 | 10 | 104279427 | missense variant | A/G;T | snv | 0.35 | 25 | ||
rs6466135 | 0.925 | 0.120 | 7 | 106861053 | upstream gene variant | A/G | snv | 0.71 | 2 | ||
rs17037102 | 0.807 | 0.240 | 4 | 106924637 | missense variant | C/A;T | snv | 0.15 | 6 | ||
rs78971134 | 1.000 | 0.120 | 12 | 107258753 | intergenic variant | A/G | snv | 7.7E-02 | 1 |