Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10087900 | 8 | 143221248 | downstream gene variant | G/A | snv | 0.37 | 1 | ||||
rs10091038 | 8 | 29502788 | intergenic variant | A/C | snv | 0.57 | 1 | ||||
rs10198423 | 2 | 85333439 | upstream gene variant | G/A;C;T | snv | 1 | |||||
rs1026422 | 7 | 50280211 | upstream gene variant | G/A | snv | 0.51 | 1 | ||||
rs10479024 | 5 | 133131681 | intergenic variant | C/A;T | snv | 1 | |||||
rs10836699 | 11 | 37162788 | intergenic variant | C/T | snv | 0.33 | 1 | ||||
rs1084651 | 6 | 160668785 | intron variant | G/A | snv | 0.23 | 1 | ||||
rs10874777 | 1 | 93396463 | intergenic variant | T/A;C | snv | 1 | |||||
rs11045163 | 12 | 20310592 | intergenic variant | A/G | snv | 0.38 | 1 | ||||
rs11045171 | 12 | 20317265 | intergenic variant | A/G | snv | 0.16 | 1 | ||||
rs11067829 | 12 | 109679067 | regulatory region variant | A/G | snv | 0.23 | 1 | ||||
rs11082766 | 18 | 49606094 | intergenic variant | C/T | snv | 4.4E-02 | 1 | ||||
rs11218720 | 11 | 122633992 | intergenic variant | A/G | snv | 0.39 | 1 | ||||
rs11236520 | 11 | 75749624 | intergenic variant | G/A | snv | 0.11 | 1 | ||||
rs11246602 | 11 | 54607190 | upstream gene variant | A/G | snv | 0.11 | 1 | ||||
rs11434755 | 11 | 18045473 | upstream gene variant | -/A | delins | 0.41 | 1 | ||||
rs114529226 | 14 | 106368436 | upstream gene variant | G/A | snv | 4.3E-02 | 1 | ||||
rs116569761 | 6 | 32680379 | intergenic variant | G/A | snv | 1 | |||||
rs11782435 | 8 | 13678606 | intergenic variant | C/T | snv | 0.16 | 1 | ||||
rs11986942 | 1.000 | 0.040 | 8 | 20009934 | intergenic variant | C/G;T | snv | 1 | |||
rs12226802 | 11 | 55556832 | downstream gene variant | A/G | snv | 0.10 | 1 | ||||
rs12575459 | 11 | 58394909 | regulatory region variant | G/A | snv | 5.2E-02 | 1 | ||||
rs1263173 | 0.925 | 0.080 | 11 | 116810292 | downstream gene variant | G/A | snv | 0.53 | 1 | ||
rs12740061 | 1 | 68942127 | intron variant | C/A;T | snv | 1 | |||||
rs1281955 | 6 | 153138309 | intergenic variant | T/A | snv | 0.43 | 1 |