Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6951457 | 1.000 | 0.040 | 7 | 107815875 | intergenic variant | G/A;C | snv | 1 | |||
rs6466198 | 0.827 | 0.120 | 7 | 107839681 | regulatory region variant | A/T | snv | 0.68 | 5 | ||
rs4380874 | 1.000 | 0.040 | 7 | 107839870 | intergenic variant | T/A;C;G | snv | 2 | |||
rs4510766 | 1.000 | 0.040 | 7 | 107852344 | intergenic variant | A/G | snv | 0.36 | 1 | ||
rs886774 | 1.000 | 0.040 | 7 | 107854989 | regulatory region variant | G/A | snv | 0.67 | 1 | ||
rs4598195 | 1.000 | 0.040 | 7 | 107862996 | intergenic variant | A/C | snv | 0.34 | 1 | ||
rs7115956 | 0.827 | 0.120 | 11 | 110085620 | intron variant | C/T | snv | 0.38 | 5 | ||
rs4561177 | 0.807 | 0.120 | 11 | 110091706 | intron variant | A/G | snv | 0.36 | 6 | ||
rs8061882 | 0.827 | 0.120 | 16 | 11067551 | intron variant | G/C | snv | 0.11 | 5 | ||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs3851228 | 0.925 | 0.040 | 6 | 111526988 | intron variant | A/T | snv | 9.7E-02 | 3 | ||
rs360718 | 0.827 | 0.120 | 11 | 112164016 | 5 prime UTR variant | A/C | snv | 0.26 | 5 | ||
rs187238 | 0.602 | 0.680 | 11 | 112164265 | intron variant | C/A;G | snv | 48 | |||
rs1946518 | 0.602 | 0.760 | 11 | 112164735 | intron variant | T/G | snv | 0.60 | 46 | ||
rs11649613 | 0.827 | 0.120 | 16 | 11225500 | downstream gene variant | C/T | snv | 0.37 | 5 | ||
rs2024092 | 0.827 | 0.120 | 19 | 1124032 | intron variant | G/A | snv | 0.24 | 0.26 | 6 | |
rs367569 | 0.807 | 0.120 | 16 | 11271643 | intron variant | C/T | snv | 0.32 | 6 | ||
rs1143627 | 0.605 | 0.760 | 2 | 112836810 | 5 prime UTR variant | G/A | snv | 0.56 | 47 | ||
rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 92 | ||
rs4848306 | 0.851 | 0.120 | 2 | 112840530 | non coding transcript exon variant | G/A | snv | 0.39 | 6 | ||
rs3814570 | 0.925 | 0.040 | 10 | 112948751 | upstream gene variant | C/T | snv | 0.23 | 2 | ||
rs4251961 | 0.763 | 0.200 | 2 | 113116890 | intron variant | T/C | snv | 0.29 | 10 | ||
rs315952 | 0.763 | 0.400 | 2 | 113132727 | missense variant | T/A;C | snv | 4.0E-06; 0.31 | 10 | ||
rs315951 | 0.925 | 0.160 | 2 | 113133009 | 3 prime UTR variant | C/G | snv | 0.34 | 2 | ||
rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 26 |