Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1526692 | 4 | 71713007 | intergenic variant | A/G | snv | 0.41 | 2 | ||||
rs1607741 | 4 | 71853316 | intergenic variant | G/C | snv | 0.65 | 2 | ||||
rs17767445 | 4 | 71879550 | intergenic variant | G/A | snv | 0.20 | 2 | ||||
rs6730714 | 2 | 222184302 | intergenic variant | G/A;T | snv | 2 | |||||
rs719700 | 12 | 45635426 | intergenic variant | T/C | snv | 1.8E-02 | 2 | ||||
rs79666294 | 5 | 155047146 | regulatory region variant | C/T | snv | 2.2E-02 | 2 | ||||
rs79761689 | 4 | 72005565 | intergenic variant | T/C | snv | 3.7E-02 | 2 | ||||
rs10745742 | 12 | 95964751 | intron variant | C/T | snv | 0.48 | 2 | ||||
rs55665837 | 11 | 14473503 | intron variant | C/G;T | snv | 2 | |||||
rs117913124 | 11 | 14879385 | synonymous variant | G/A | snv | 1.7E-02 | 1.6E-02 | 2 | |||
rs185378533 | 11 | 71422087 | intron variant | A/G | snv | 0.68 | 2 | ||||
rs843005 | 4 | 71750610 | intron variant | C/A;T | snv | 2 | |||||
rs2277458 | 14 | 39114277 | 5 prime UTR variant | A/G | snv | 0.80 | 0.83 | 2 | |||
rs3819817 | 12 | 95984993 | intron variant | C/T | snv | 0.50 | 2 | ||||
rs2207173 | 20 | 22824423 | intergenic variant | G/A | snv | 0.72 | 2 | ||||
rs156299 | 7 | 24185113 | intergenic variant | T/G | snv | 0.53 | 2 | ||||
rs4423214 | 11 | 71462208 | intron variant | C/T | snv | 0.58 | 2 | ||||
rs4944062 | 11 | 71476248 | 3 prime UTR variant | G/A;T | snv | 2 | |||||
rs7938885 | 11 | 71458997 | non coding transcript exon variant | T/C | snv | 0.59 | 2 | ||||
rs13107347 | 4 | 72109031 | intron variant | T/C | snv | 0.32 | 2 | ||||
rs1007392 | 11 | 14753045 | intron variant | A/G | snv | 0.35 | 2 | ||||
rs11023332 | 11 | 14762564 | intron variant | G/C | snv | 0.35 | 2 | ||||
rs116970203 | 11 | 14855172 | intron variant | G/A | snv | 2.2E-02 | 2 | ||||
rs182244780 | 11 | 14363985 | intron variant | G/A | snv | 6.0E-03 | 2 | ||||
rs8018720 | 14 | 39086981 | missense variant | G/C;T | snv | 0.80; 1.1E-04 | 2 |