Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1250550 | 0.851 | 0.240 | 10 | 79300560 | intron variant | C/A | snv | 0.27 | 5 | ||
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 4 | |
rs1439112 | 0.851 | 0.160 | 2 | 134305027 | intron variant | G/A | snv | 0.61 | 4 | ||
rs2425752 | 0.851 | 0.160 | 20 | 46073481 | intron variant | T/C | snv | 0.79 | 4 | ||
rs2777899 | 0.851 | 0.160 | 17 | 59755030 | intron variant | T/A;G | snv | 4 | |||
rs497309 | 0.882 | 0.240 | 6 | 31924707 | intron variant | A/C;G | snv | 3 | |||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 3 | ||
rs1444766 | 0.882 | 0.160 | 3 | 124206424 | intron variant | A/G;T | snv | 3 | |||
rs1323292 | 0.882 | 0.160 | 1 | 192571891 | intron variant | G/A | snv | 0.86 | 3 | ||
rs1364229 | 0.925 | 0.200 | 16 | 62594871 | upstream gene variant | T/C | snv | 0.12 | 2 | ||
rs7382170 | 0.925 | 0.160 | 6 | 16970739 | intergenic variant | C/A | snv | 0.37 | 2 | ||
rs16947122 | 0.925 | 0.200 | 12 | 116928726 | intron variant | C/T | snv | 7.3E-02 | 2 | ||
rs9808753 | 0.701 | 0.400 | 21 | 33415005 | missense variant | A/G | snv | 0.20 | 0.18 | 2 | |
rs2941509 | 0.925 | 0.160 | 17 | 39764941 | 3 prime UTR variant | T/C | snv | 0.91 | 2 | ||
rs1107345 | 0.925 | 0.160 | 10 | 6045332 | intron variant | G/T | snv | 0.18 | 2 | ||
rs8021741 | 0.925 | 0.160 | 14 | 75556057 | intergenic variant | T/G | snv | 0.30 | 2 | ||
rs6062314 | 0.925 | 0.160 | 20 | 63778360 | intron variant | C/G;T | snv | 2 | |||
rs2922994 | 1.000 | 0.120 | 6 | 31368124 | intron variant | A/G | snv | 9.0E-02 | 1 | ||
rs9461741 | 1.000 | 0.120 | 6 | 32402810 | intron variant | G/C | snv | 3.8E-02 | 1 |