Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 52 | |
rs2395185 | 0.724 | 0.360 | 6 | 32465390 | intron variant | G/T | snv | 0.29 | 17 | ||
rs1057520009 | 0.790 | 0.200 | 2 | 61492337 | missense variant | C/T | snv | 4.4E-06 | 14 | ||
rs6903608 | 0.742 | 0.400 | 6 | 32460508 | intron variant | C/G;T | snv | 11 | |||
rs2248462 | 0.807 | 0.240 | 6 | 31479019 | downstream gene variant | G/A | snv | 0.19 | 10 | ||
rs2734986 | 0.827 | 0.160 | 6 | 29850791 | intron variant | T/C | snv | 0.10 | 5 | ||
rs27524 | 0.851 | 0.160 | 5 | 96766240 | intron variant | A/G | snv | 0.61 | 4 | ||
rs6904029 | 0.851 | 0.200 | 6 | 29975290 | non coding transcript exon variant | G/A | snv | 0.29 | 0.26 | 4 | |
rs10813831 | 0.925 | 0.120 | 9 | 32526148 | missense variant | G/A | snv | 0.21 | 0.24 | 2 | |
rs6457715 | 0.925 | 0.120 | 6 | 33115411 | intron variant | A/G | snv | 0.35 | 2 |