Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7097656 | 0.827 | 0.120 | 10 | 80491075 | intron variant | T/C;G | snv | 6 | |||
rs6586030 | 1.000 | 0.040 | 10 | 80494291 | intron variant | A/G;T | snv | 2 | |||
rs1993484 | 10 | 80462942 | intron variant | T/C | snv | 0.82 | 1 | ||||
rs7086627 | 10 | 80460841 | intron variant | C/T | snv | 0.80 | 1 | ||||
rs7100689 | 10 | 80462422 | intron variant | C/A;G | snv | 1 | |||||
rs12220642 | 10 | 80459208 | intron variant | T/C;G | snv | 1 | |||||
rs1902661 | 1.000 | 0.040 | 10 | 80458350 | intron variant | G/A;C | snv | 1 | |||
rs10788639 | 10 | 80473469 | intron variant | C/G | snv | 0.64 | 1 | ||||
rs17680741 | 1.000 | 0.040 | 10 | 80491758 | intron variant | T/C | snv | 0.25 | 1 | ||
rs12264252 | 1.000 | 0.040 | 10 | 80517585 | intron variant | G/A | snv | 0.18 | 1 |