Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2046210 | 0.708 | 0.280 | 6 | 151627231 | intergenic variant | G/A | snv | 0.41 | 21 | ||
rs2073618 | 0.716 | 0.480 | 8 | 118951813 | missense variant | G/C | snv | 0.52 | 0.60 | 19 | |
rs3736228 | 0.752 | 0.400 | 11 | 68433827 | missense variant | C/T | snv | 0.13 | 0.11 | 13 | |
rs34920465 | 0.807 | 0.160 | 1 | 22373858 | intergenic variant | A/G | snv | 0.24 | 9 | ||
rs2073617 | 0.776 | 0.360 | 8 | 118952044 | upstream gene variant | G/A | snv | 0.58 | 9 | ||
rs754388 | 0.882 | 0.120 | 14 | 92649065 | intron variant | G/C;T | snv | 7 | |||
rs34670419 | 1.000 | 0.080 | 7 | 99533211 | 3 prime UTR variant | G/A;T | snv | 7.7E-06; 2.6E-02 | 7 | ||
rs6929137 | 0.851 | 0.160 | 6 | 151615542 | missense variant | G/A | snv | 0.31 | 0.36 | 6 | |
rs1864325 | 0.882 | 0.160 | 17 | 45900461 | intron variant | C/T | snv | 0.14 | 6 | ||
rs2252865 | 0.851 | 0.040 | 1 | 8362616 | intron variant | T/C | snv | 0.72 | 6 | ||
rs4355801 | 0.882 | 0.120 | 8 | 118911634 | regulatory region variant | A/G;T | snv | 5 | |||
rs7524102 | 0.882 | 0.160 | 1 | 22371954 | intergenic variant | A/G | snv | 0.21 | 5 | ||
rs9921222 | 0.925 | 0.120 | 16 | 325782 | intron variant | C/T | snv | 0.51 | 5 | ||
rs9303521 | 0.925 | 0.120 | 17 | 45727828 | intron variant | T/C;G | snv | 0.60 | 5 | ||
rs3130340 | 0.851 | 0.200 | 6 | 32276850 | intron variant | T/C | snv | 0.25 | 5 | ||
rs12568930 | 1.000 | 0.040 | 1 | 22375738 | intergenic variant | T/C | snv | 0.21 | 4 | ||
rs3018362 | 0.882 | 0.120 | 18 | 62414860 | upstream gene variant | A/G | snv | 0.67 | 4 | ||
rs6684375 | 1 | 22379941 | regulatory region variant | C/T | snv | 0.20 | 4 | ||||
rs6959212 | 7 | 38088724 | intergenic variant | T/C;G | snv | 4 | |||||
rs1038304 | 0.882 | 0.160 | 6 | 151612040 | intron variant | A/G | snv | 0.58 | 4 | ||
rs2414095 | 15 | 51232095 | intron variant | A/G | snv | 0.69 | 4 | ||||
rs7776725 | 1.000 | 0.080 | 7 | 121393067 | intron variant | T/C | snv | 0.28 | 4 | ||
rs3755955 | 0.925 | 0.080 | 4 | 1000626 | missense variant | G/A;C | snv | 0.16; 8.0E-06 | 4 | ||
rs6831280 | 0.925 | 0.080 | 4 | 1002377 | missense variant | G/A;C | snv | 0.17 | 4 | ||
rs7521902 | 1.000 | 0.040 | 1 | 22164231 | intergenic variant | C/A | snv | 0.22 | 4 |