Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
rs878854066 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 213 | |||
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
rs1051740 | 0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 | 56 | |
rs144848 | 0.653 | 0.440 | 13 | 32332592 | missense variant | A/C | snv | 0.28 | 0.23 | 29 | |
rs4977756 | 0.683 | 0.440 | 9 | 22068653 | intron variant | G/A | snv | 0.64 | 24 | ||
rs1063192 | 0.695 | 0.520 | 9 | 22003368 | 3 prime UTR variant | G/A;T | snv | 24 | |||
rs121918457 | 0.701 | 0.280 | 12 | 112488466 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 24 | |
rs61754966 | 0.701 | 0.280 | 8 | 89978293 | missense variant | T/C;G | snv | 1.2E-03 | 23 | ||
rs879255280 | 0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv | 22 | |||
rs2157719 | 0.708 | 0.360 | 9 | 22033367 | non coding transcript exon variant | C/T | snv | 0.71 | 17 | ||
rs3734254 | 0.752 | 0.240 | 6 | 35427233 | 3 prime UTR variant | C/T | snv | 0.69 | 14 | ||
rs80358638 | 0.776 | 0.280 | 13 | 32338277 | stop gained | G/A;T | snv | 5.6E-05 | 9 | ||
rs63750451 | 0.827 | 0.160 | 7 | 5986883 | stop gained | G/A;C | snv | 1.6E-05 | 7 | ||
rs143277125 | 0.851 | 0.160 | 7 | 5992012 | stop gained | G/A;T | snv | 4.0E-06 | 6 | ||
rs13306747 | 0.807 | 0.200 | 3 | 12416775 | synonymous variant | C/A;G;T | snv | 8.0E-06; 4.2E-03; 7.2E-05 | 6 | ||
rs922324159 | 0.827 | 0.040 | 2 | 15941962 | 5 prime UTR variant | G/A | snv | 2.4E-04 | 5 | ||
rs1400239417 | 0.882 | 0.040 | 2 | 29220756 | missense variant | T/A;G | snv | 4.0E-06 | 2.1E-05 | 4 | |
rs755103500 | 0.851 | 0.160 | 9 | 95516820 | start lost | T/C;G | snv | 8.4E-06; 4.2E-06 | 4 | ||
rs766905791 | 0.851 | 0.160 | 9 | 95485815 | start lost | T/C | snv | 1.2E-05 | 4 | ||
rs765602971 | 0.882 | 0.040 | 8 | 89970503 | missense variant | T/C | snv | 4.0E-06 | 3 | ||
rs6008197 | 0.882 | 0.040 | 22 | 46224519 | intron variant | G/C | snv | 0.27 | 3 |