Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11099097 | 4 | 80246155 | intergenic variant | C/T | snv | 0.30 | 6 | ||||
rs11953630 | 5 | 158418394 | intergenic variant | C/A;T | snv | 6 | |||||
rs1887320 | 20 | 10985350 | intron variant | G/A | snv | 0.46 | 6 | ||||
rs17035646 | 1 | 10736490 | intron variant | G/A;T | snv | 6 | |||||
rs10255839 | 7 | 27249498 | intron variant | G/A | snv | 0.87 | 6 | ||||
rs1290784 | 3 | 169379112 | intron variant | C/A;T | snv | 6 | |||||
rs419076 | 3 | 169383098 | intron variant | T/A;C | snv | 6 | |||||
rs932764 | 10 | 94136183 | intron variant | A/G | snv | 0.38 | 6 | ||||
rs381815 | 1.000 | 0.040 | 11 | 16880721 | intron variant | C/A;T | snv | 0.24 | 6 | ||
rs35441 | 12 | 115115310 | intergenic variant | C/T | snv | 0.40 | 5 | ||||
rs4373814 | 10 | 18131043 | intergenic variant | G/C;T | snv | 5 | |||||
rs438885 | 2 | 164195781 | intron variant | A/T | snv | 0.56 | 5 | ||||
rs5883070 | 7 | 27240226 | intron variant | -/AAAACA;AACA | delins | 0.91 | 5 | ||||
rs12946454 | 0.925 | 0.040 | 17 | 45130754 | intron variant | A/T | snv | 0.21 | 5 | ||
rs7129220 | 11 | 10328991 | intron variant | G/A | snv | 0.10 | 5 | ||||
rs4590817 | 10 | 61707795 | intron variant | G/C | snv | 0.15 | 5 | ||||
rs1813353 | 10 | 18418519 | intron variant | T/C | snv | 0.29 | 5 | ||||
rs1573643 | 15 | 90877743 | intron variant | T/C | snv | 0.33 | 5 | ||||
rs1731249 | 2 | 26697157 | intron variant | T/A | snv | 0.48 | 5 | ||||
rs11636952 | 15 | 74821981 | intron variant | T/C | snv | 0.48 | 5 | ||||
rs448378 | 1.000 | 0.040 | 3 | 169383111 | intron variant | G/A;C | snv | 5 | |||
rs62434109 | 6 | 150654176 | intron variant | T/G | snv | 8.4E-02 | 5 | ||||
rs12940887 | 17 | 49325445 | intron variant | C/T | snv | 0.28 | 5 | ||||
rs2392929 | 7 | 106773623 | upstream gene variant | T/A;C;G | snv | 4 | |||||
rs2484294 | 10 | 114032303 | intergenic variant | G/A | snv | 0.70 | 4 |