Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4444235 | 0.701 | 0.240 | 14 | 53944201 | downstream gene variant | T/C | snv | 0.43 | 23 | ||
rs16892766 | 0.716 | 0.240 | 8 | 116618444 | intergenic variant | A/C | snv | 9.3E-02 | 18 | ||
rs4779584 | 0.732 | 0.160 | 15 | 32702555 | intergenic variant | T/C | snv | 0.67 | 16 | ||
rs1321311 | 0.742 | 0.160 | 6 | 36655123 | regulatory region variant | C/A | snv | 0.28 | 15 | ||
rs2808630 | 0.742 | 0.240 | 1 | 159711078 | downstream gene variant | C/T | snv | 0.77 | 13 | ||
rs6691170 | 0.776 | 0.080 | 1 | 221872104 | intergenic variant | G/T | snv | 0.34 | 12 | ||
rs6687758 | 0.763 | 0.200 | 1 | 221991606 | regulatory region variant | A/G | snv | 0.20 | 11 | ||
rs2965667 | 0.776 | 0.080 | 12 | 17291799 | intergenic variant | A/T | snv | 0.96 | 10 | ||
rs4242382 | 0.763 | 0.240 | 8 | 127505328 | intergenic variant | A/G;T | snv | 9 | |||
rs10090154 | 0.807 | 0.160 | 8 | 127519892 | intergenic variant | T/A;C | snv | 7 | |||
rs2555639 | 0.851 | 0.080 | 4 | 174540379 | non coding transcript exon variant | T/C | snv | 0.38 | 7 | ||
rs719725 | 0.827 | 0.080 | 9 | 6365683 | intergenic variant | A/C | snv | 0.34 | 7 | ||
rs1924966 | 0.807 | 0.080 | 13 | 72432915 | intergenic variant | T/G | snv | 0.33 | 6 | ||
rs6854845 | 0.827 | 0.080 | 4 | 74821455 | intergenic variant | G/T | snv | 0.13 | 6 | ||
rs12413624 | 0.851 | 0.120 | 10 | 118519432 | intergenic variant | T/A | snv | 0.34 | 5 | ||
rs1088967 | 0.851 | 0.080 | X | 127010099 | intergenic variant | T/A;C | snv | 4 | |||
rs1535989 | 0.925 | 0.080 | 13 | 105370372 | intergenic variant | A/G;T | snv | 4 | |||
rs1194338 | 0.925 | 0.080 | 11 | 65493967 | upstream gene variant | C/A;T | snv | 3 | |||
rs180040 | 0.882 | 0.120 | 15 | 97027933 | intergenic variant | T/C | snv | 0.85 | 3 | ||
rs7163702 | 0.925 | 0.080 | 15 | 28460135 | upstream gene variant | C/A | snv | 2 | |||
rs722025 | 0.925 | 0.080 | 5 | 8107899 | intergenic variant | A/G | snv | 0.27 | 2 | ||
rs823920 | 0.925 | 0.080 | 9 | 101900303 | intergenic variant | A/G | snv | 0.12 | 2 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 |