Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6822844 | 0.689 | 0.520 | 4 | 122588266 | regulatory region variant | G/T | snv | 0.10 | 19 | ||
rs4444235 | 0.701 | 0.240 | 14 | 53944201 | downstream gene variant | T/C | snv | 0.43 | 15 | ||
rs2808630 | 0.742 | 0.240 | 1 | 159711078 | downstream gene variant | C/T | snv | 0.77 | 13 | ||
rs16892766 | 0.716 | 0.240 | 8 | 116618444 | intergenic variant | A/C | snv | 9.3E-02 | 10 | ||
rs2069514 | 0.807 | 0.160 | 15 | 74745879 | upstream gene variant | G/A | snv | 0.13 | 9 | ||
rs6920220 | 0.742 | 0.440 | 6 | 137685367 | intron variant | G/A | snv | 0.16 | 9 | ||
rs3865188 | 0.790 | 0.320 | 16 | 82617112 | intergenic variant | A/G;T | snv | 8 | |||
rs4242382 | 0.763 | 0.240 | 8 | 127505328 | intergenic variant | A/G;T | snv | 8 | |||
rs4779584 | 0.732 | 0.160 | 15 | 32702555 | intergenic variant | T/C | snv | 0.67 | 8 | ||
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 | ||
rs3024505 | 0.790 | 0.320 | 1 | 206766559 | upstream gene variant | G/A | snv | 0.11 | 7 | ||
rs6013897 | 0.790 | 0.200 | 20 | 54125940 | regulatory region variant | T/A | snv | 0.23 | 7 | ||
rs719725 | 0.827 | 0.080 | 9 | 6365683 | intergenic variant | A/C | snv | 0.34 | 7 | ||
rs961253 | 0.732 | 0.240 | 20 | 6423634 | intergenic variant | C/A | snv | 0.34 | 7 | ||
rs1321311 | 0.742 | 0.160 | 6 | 36655123 | regulatory region variant | C/A | snv | 0.28 | 6 | ||
rs1924966 | 0.807 | 0.080 | 13 | 72432915 | intergenic variant | T/G | snv | 0.33 | 6 | ||
rs4848306 | 0.851 | 0.120 | 2 | 112840530 | non coding transcript exon variant | G/A | snv | 0.39 | 6 | ||
rs7553007 | 0.827 | 0.120 | 1 | 159728759 | intergenic variant | G/A | snv | 0.31 | 6 | ||
rs406193 | 0.882 | 0.120 | 20 | 32811837 | downstream gene variant | T/C | snv | 0.91 | 5 | ||
rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 5 | ||
rs1088967 | 0.851 | 0.080 | X | 127010099 | intergenic variant | T/A;C | snv | 4 | |||
rs11676348 | 0.790 | 0.160 | 2 | 218145423 | regulatory region variant | C/G;T | snv | 4 | |||
rs1535989 | 0.925 | 0.080 | 13 | 105370372 | intergenic variant | A/G;T | snv | 4 | |||
rs2069521 | 0.851 | 0.240 | 15 | 74746626 | upstream gene variant | G/A | snv | 4.9E-02 | 4 |