Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs148704956 | 0.716 | 0.360 | 6 | 52187772 | missense variant | A/G | snv | 8.0E-06 | 7.0E-06 | 19 | |
rs4975616 | 0.763 | 0.320 | 5 | 1315545 | downstream gene variant | G/A | snv | 0.51 | 12 | ||
rs1864183 | 0.742 | 0.240 | 5 | 82253397 | missense variant | C/T | snv | 0.52 | 0.40 | 12 | |
rs989902 | 0.742 | 0.240 | 4 | 86785353 | missense variant | T/G | snv | 0.42 | 0.53 | 12 | |
rs28366003 | 0.763 | 0.240 | 16 | 56608579 | upstream gene variant | A/C;G | snv | 4.6E-02 | 10 | ||
rs115160714 | 0.807 | 0.200 | 3 | 133601021 | 3 prime UTR variant | G/A | snv | 5.8E-03 | 9 | ||
rs6877842 | 0.807 | 0.320 | 5 | 31532531 | intron variant | G/C | snv | 0.16 | 7 | ||
rs820196 | 0.807 | 0.160 | 17 | 75631459 | missense variant | T/A;C | snv | 1.6E-05; 0.26 | 6 | ||
rs5744455 | 0.882 | 0.160 | 5 | 140633722 | upstream gene variant | G/A;T | snv | 5 | |||
rs13078 | 0.827 | 0.280 | 14 | 95090410 | 3 prime UTR variant | A/T | snv | 0.85 | 5 | ||
rs2230600 | 0.827 | 0.160 | 4 | 86769845 | missense variant | A/G | snv | 0.18 | 0.14 | 5 | |
rs4789223 | 0.851 | 0.120 | 17 | 75645819 | intron variant | G/A | snv | 0.46 | 4 | ||
rs4253211 | 0.882 | 0.240 | 10 | 49470271 | missense variant | C/G;T | snv | 7.1E-02; 2.0E-05 | 3 | ||
rs1816158 | 0.925 | 0.200 | 11 | 122155752 | intron variant | C/A;T | snv | 3 | |||
rs3213282 | 0.882 | 0.160 | 19 | 43568728 | intron variant | G/C | snv | 0.57 | 3 | ||
rs3810378 | 1.000 | 0.120 | 19 | 43577449 | intron variant | G/C | snv | 0.29 | 3 | ||
rs748148861 | 0.925 | 0.120 | 6 | 167136856 | missense variant | G/C | snv | 8.0E-06 | 2 | ||
rs50871 | 0.925 | 0.120 | 19 | 45359257 | intron variant | C/A | snv | 0.64 | 2 | ||
rs4725443 | 0.925 | 0.120 | 7 | 152170176 | intron variant | T/C | snv | 9.3E-02 | 2 | ||
rs6464211 | 0.925 | 0.160 | 7 | 152176768 | synonymous variant | C/T | snv | 0.24 | 0.34 | 2 | |
rs6943984 | 0.925 | 0.120 | 7 | 152201919 | intron variant | G/A | snv | 0.11 | 2 | ||
rs28903090 | 0.925 | 0.120 | 5 | 132587981 | missense variant | G/T | snv | 1.2E-03 | 1.4E-03 | 2 | |
rs56161233 | 0.925 | 0.120 | 2 | 235055489 | 3 prime UTR variant | C/T | snv | 0.11 | 2 | ||
rs865789884 | 0.925 | 0.120 | 8 | 23145778 | missense variant | G/A;C | snv | 4.0E-06 | 2 | ||
rs1799778 | 1.000 | 0.120 | 19 | 43554989 | intron variant | G/T | snv | 0.31 | 1 |