Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 30 | ||
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 26 | |
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 20 | |
rs4803750 | 0.807 | 0.240 | 19 | 44744370 | upstream gene variant | A/G | snv | 7.7E-02 | 19 | ||
rs2740488 | 0.827 | 0.120 | 9 | 104899461 | intron variant | A/C | snv | 0.29 | 9 | ||
rs769449 | 0.882 | 0.120 | 19 | 44906745 | non coding transcript exon variant | G/A | snv | 8.4E-02 | 8 | ||
rs56131196 | 0.925 | 0.160 | 19 | 44919589 | downstream gene variant | G/A | snv | 0.18 | 6 | ||
rs157582 | 0.851 | 0.160 | 19 | 44892962 | intron variant | C/T | snv | 0.24 | 0.29 | 5 | |
rs2678379 | 1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 | 5 | ||
rs157580 | 0.882 | 0.160 | 19 | 44892009 | intron variant | G/A | snv | 0.69 | 4 | ||
rs261291 | 1.000 | 0.080 | 15 | 58387979 | intron variant | T/A;C | snv | 4 | |||
rs439401 | 0.851 | 0.200 | 19 | 44911194 | non coding transcript exon variant | T/C | snv | 0.68 | 3 | ||
rs483082 | 1.000 | 0.080 | 19 | 44912921 | non coding transcript exon variant | G/T | snv | 0.28 | 3 | ||
rs75627662 | 1.000 | 0.080 | 19 | 44910319 | non coding transcript exon variant | C/T | snv | 0.17 | 3 |