Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 19 | ||
rs543874 | 1.000 | 0.080 | 1 | 177920345 | upstream gene variant | A/G | snv | 0.21 | 8 | ||
rs34517439 | 0.882 | 0.120 | 1 | 77984833 | intron variant | C/A | snv | 7.3E-02 | 7 | ||
rs7531118 | 1.000 | 0.080 | 1 | 72371556 | intron variant | T/C | snv | 0.40 | 7 | ||
rs12140153 | 1 | 62114219 | missense variant | G/A;T | snv | 4.0E-06; 5.9E-02 | 5 | ||||
rs3101336 | 1.000 | 0.080 | 1 | 72285502 | intron variant | T/C | snv | 0.62 | 5 | ||
rs4130548 | 1.000 | 0.040 | 1 | 77998184 | intron variant | T/C | snv | 0.25 | 5 | ||
rs633715 | 1.000 | 0.080 | 1 | 177883445 | intron variant | T/C | snv | 0.17 | 5 | ||
rs11161721 | 1 | 86022231 | intron variant | C/A | snv | 0.27 | 0.27 | 4 | |||
rs17024393 | 1 | 109612066 | intron variant | T/C | snv | 4.6E-02 | 4 | ||||
rs2296172 | 1.000 | 0.080 | 1 | 39370145 | missense variant | A/G;T | snv | 0.19; 8.0E-06 | 4 | ||
rs2568958 | 0.882 | 0.160 | 1 | 72299433 | intron variant | G/A;C | snv | 4 | |||
rs34720381 | 1 | 171486183 | intron variant | C/T | snv | 7.3E-02 | 4 | ||||
rs545608 | 0.925 | 0.040 | 1 | 177929986 | intron variant | G/C | snv | 0.20 | 4 | ||
rs10913469 | 1.000 | 0.080 | 1 | 177944384 | intron variant | T/C | snv | 0.22 | 3 | ||
rs10923724 | 1 | 119004219 | upstream gene variant | C/T | snv | 0.53 | 3 | ||||
rs11209951 | 1 | 72371807 | intron variant | C/T | snv | 0.61 | 3 | ||||
rs113722913 | 1 | 199950846 | intergenic variant | T/C | snv | 2.6E-02 | 3 | ||||
rs12128108 | 0.925 | 0.040 | 1 | 49827749 | intron variant | C/G;T | snv | 3 | |||
rs17381664 | 1.000 | 0.080 | 1 | 77582646 | intron variant | T/C | snv | 0.29 | 3 | ||
rs1993709 | 1.000 | 0.080 | 1 | 72372846 | intron variant | A/G | snv | 0.85 | 3 | ||
rs2785980 | 1 | 219527177 | intergenic variant | T/C | snv | 0.28 | 3 | ||||
rs2820292 | 1 | 201815159 | intron variant | A/C | snv | 0.48 | 3 | ||||
rs2820315 | 0.882 | 0.040 | 1 | 201903136 | intron variant | C/T | snv | 0.23 | 3 | ||
rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 3 |