Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35736272 | 0.807 | 0.160 | 17 | 39876427 | intron variant | T/C | snv | 0.35 | 5 | ||
rs259964 | 0.827 | 0.120 | 20 | 59249254 | intron variant | A/G;T | snv | 6 | |||
rs10761648 | 0.827 | 0.120 | 10 | 62594503 | intron variant | C/T | snv | 0.20 | 5 | ||
rs7915475 | 0.827 | 0.120 | 10 | 62621908 | intron variant | A/G | snv | 0.28 | 5 | ||
rs1250573 | 0.827 | 0.120 | 10 | 79282718 | intron variant | G/A | snv | 0.23 | 5 | ||
rs140135 | 0.827 | 0.120 | 22 | 29767846 | non coding transcript exon variant | C/G | snv | 0.79 | 5 | ||
rs2266961 | 0.807 | 0.160 | 22 | 21574308 | intron variant | C/G | snv | 0.18 | 6 | ||
rs1893592 | 0.742 | 0.280 | 21 | 42434957 | missense variant | A/C;G | snv | 0.27; 8.0E-06 | 7 | ||
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 7 | ||
rs35018800 | 0.790 | 0.160 | 19 | 10354167 | missense variant | G/A | snv | 4.6E-03 | 4.9E-03 | 5 | |
rs7097656 | 0.827 | 0.120 | 10 | 80491075 | intron variant | T/C;G | snv | 6 | |||
rs74817271 | 0.807 | 0.120 | 5 | 151090412 | intron variant | G/A | snv | 5.0E-02 | 6 | ||
rs7848647 | 0.732 | 0.320 | 9 | 114806766 | upstream gene variant | T/C | snv | 0.74 | 6 | ||
rs6062496 | 0.827 | 0.120 | 20 | 63697746 | intron variant | G/A | snv | 0.52 | 6 | ||
rs1860545 | 0.790 | 0.200 | 12 | 6337611 | intron variant | G/A | snv | 0.31 | 5 | ||
rs2234161 | 0.827 | 0.120 | 1 | 2559766 | non coding transcript exon variant | C/T | snv | 4.1E-05; 0.55 | 0.58 | 5 | |
rs582757 | 0.776 | 0.320 | 6 | 137876687 | intron variant | C/T | snv | 0.70 | 5 | ||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 6 | ||
rs77981966 | 0.827 | 0.120 | 2 | 43550825 | intron variant | C/T | snv | 4.6E-02 | 5 | ||
rs11691685 | 0.827 | 0.120 | 2 | 144724260 | intron variant | A/G | snv | 5.2E-02 | 5 | ||
rs72977586 | 0.827 | 0.120 | 19 | 1186317 | intron variant | G/C | snv | 0.16 | 5 | ||
rs12942547 | 0.807 | 0.200 | 17 | 42375526 | intron variant | A/G;T | snv | 6 | |||
rs12718244 | 0.827 | 0.120 | 7 | 50136058 | intron variant | G/A | snv | 0.33 | 0.33 | 6 | |
rs12694846 | 0.827 | 0.120 | 2 | 230283413 | intron variant | A/G | snv | 0.20 | 5 | ||
rs17293632 | 0.763 | 0.240 | 15 | 67150258 | intron variant | C/T | snv | 0.17 | 8 |