Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 13 | |
rs10096777 | 8 | 10660990 | intron variant | G/A | snv | 0.61 | 2 | ||||
rs10255839 | 7 | 27249498 | intron variant | G/A | snv | 0.87 | 6 | ||||
rs10832417 | 11 | 2631427 | non coding transcript exon variant | T/G | snv | 0.32 | 3 | ||||
rs10850411 | 12 | 114949991 | intergenic variant | T/C | snv | 0.34 | 1 | ||||
rs11014166 | 0.882 | 0.040 | 10 | 18419869 | intron variant | A/T | snv | 0.27 | 10 | ||
rs11023906 | 11 | 16302860 | intron variant | G/A | snv | 0.17 | 3 | ||||
rs11099097 | 4 | 80246155 | intergenic variant | C/T | snv | 0.30 | 6 | ||||
rs11158609 | 14 | 24219608 | intron variant | G/A | snv | 0.89 | 2 | ||||
rs11191548 | 0.882 | 0.080 | 10 | 103086421 | 3 prime UTR variant | T/C | snv | 8.6E-02 | 10 | ||
rs1133322 | 15 | 74920016 | 3 prime UTR variant | A/G | snv | 0.38 | 2 | ||||
rs11636952 | 15 | 74821981 | intron variant | T/C | snv | 0.48 | 5 | ||||
rs11693319 | 2 | 178873542 | 3 prime UTR variant | C/G;T | snv | 2 | |||||
rs1173771 | 5 | 32814922 | regulatory region variant | A/G | snv | 0.65 | 9 | ||||
rs11953630 | 5 | 158418394 | intergenic variant | C/A;T | snv | 6 | |||||
rs12413409 | 0.790 | 0.200 | 10 | 102959339 | intron variant | G/A | snv | 9.0E-02 | 9 | ||
rs12705959 | 7 | 114358191 | intron variant | C/T | snv | 0.39 | 2 | ||||
rs12899430 | 15 | 74936759 | intron variant | T/C | snv | 0.37 | 2 | ||||
rs1290784 | 3 | 169379112 | intron variant | C/A;T | snv | 6 | |||||
rs12940887 | 17 | 49325445 | intron variant | C/T | snv | 0.28 | 5 | ||||
rs12946454 | 0.925 | 0.040 | 17 | 45130754 | intron variant | A/T | snv | 0.21 | 5 | ||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
rs13139571 | 1.000 | 0.040 | 4 | 155724361 | intron variant | C/A | snv | 0.22 | 9 | ||
rs13178964 | 5 | 105011948 | intron variant | A/G | snv | 0.17 | 2 | ||||
rs13255193 | 8 | 11451683 | intron variant | T/C | snv | 0.47 | 2 |