Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12041331 | 0.776 | 0.200 | 1 | 156899922 | intron variant | G/A | snv | 0.19 | 11 | ||
rs150813342 | 9 | 132989126 | synonymous variant | C/T | snv | 4.1E-03 | 4.1E-03 | 9 | |||
rs6993770 | 0.925 | 0.080 | 8 | 105569300 | intron variant | A/T | snv | 0.31 | 9 | ||
rs11082304 | 18 | 23141009 | intron variant | G/C;T | snv | 6 | |||||
rs11553699 | 12 | 121779004 | 3 prime UTR variant | A/G | snv | 9.4E-02 | 6 | ||||
rs114694170 | 1.000 | 0.040 | 5 | 88884379 | non coding transcript exon variant | T/C | snv | 3.6E-02 | 5 | ||
rs78909033 | 2 | 240571486 | intron variant | G/A | snv | 9.2E-02 | 5 | ||||
rs4432538 | 20 | 8626746 | intron variant | G/A | snv | 0.52 | 4 | ||||
rs56043070 | 1 | 247556467 | splice donor variant | G/A;T | snv | 5.2E-02; 4.1E-06 | 4 | ||||
rs1059196 | 22 | 19724571 | 3 prime UTR variant | C/T | snv | 0.42 | 3 | ||||
rs11071720 | 15 | 63049797 | intron variant | T/C;G | snv | 3 | |||||
rs117672662 | 14 | 68958750 | intron variant | T/C | snv | 7.4E-03 | 3 | ||||
rs17572109 | 2 | 218229211 | non coding transcript exon variant | G/A;T | snv | 3 | |||||
rs3804749 | 3 | 123114156 | intron variant | C/T | snv | 0.48 | 3 | ||||
rs41303899 | 20 | 59023753 | missense variant | G/A | snv | 8.7E-04 | 9.0E-04 | 3 | |||
rs41315846 | 1 | 247549001 | intron variant | T/C | snv | 0.44 | 0.52 | 3 | |||
rs4907622 | 13 | 113362571 | intron variant | G/C;T | snv | 3 | |||||
rs553749201 | 17 | 4933900 | synonymous variant | C/A | snv | 3 | |||||
rs655029 | 2 | 31254972 | intron variant | G/A | snv | 0.78 | 3 | ||||
rs7641175 | 3 | 18269920 | intron variant | G/A | snv | 0.81 | 3 | ||||
rs8073060 | 17 | 35548243 | missense variant | T/A | snv | 0.32 | 0.34 | 3 | |||
rs1060431 | 17 | 4937573 | 3 prime UTR variant | G/A | snv | 0.13 | 2 | ||||
rs10820606 | 9 | 96430637 | intergenic variant | A/C | snv | 0.23 | 2 | ||||
rs11083766 | 19 | 45212232 | intron variant | T/C | snv | 0.26 | 2 | ||||
rs111941366 | 1 | 25409878 | intron variant | C/T | snv | 0.30 | 2 |