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 | |||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 144 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 73 | |||
rs121434569 | 0.581 | 0.520 | 7 | 55181378 | missense variant | C/T | snv | 2.8E-05 | 5.6E-05 | 70 | |
rs727503094 | 0.633 | 0.440 | 11 | 534287 | missense variant | GC/AG;AT;TA;TT | mnv | 41 | |||
rs112445441 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 32 | |||
rs104894226 | 0.658 | 0.560 | 11 | 534285 | missense variant | C/A;G;T | snv | 29 | |||
rs1569686 | 0.752 | 0.400 | 20 | 32779273 | intron variant | G/A;C;T | snv | 15 | |||
rs121913513 | 0.776 | 0.120 | 4 | 54727495 | missense variant | T/C | snv | 10 | |||
rs121913517 | 0.851 | 0.120 | 4 | 54727444 | missense variant | T/A;C;G | snv | 6 | |||
rs1057519711 | 0.882 | 0.240 | 4 | 54733168 | missense variant | T/A | snv | 5 | |||
rs121913685 | 0.882 | 0.080 | 4 | 54727443 | inframe deletion | TTGTTG/-;TTG | delins | 4 | |||
rs1057519704 | 0.882 | 0.080 | 4 | 54727425 | missense variant | T/A | snv | 3 | |||
rs121913235 | 0.925 | 0.080 | 4 | 54727437 | missense variant | T/A;C;G | snv | 3 | |||
rs1222380251 | 0.925 | 0.080 | 5 | 56875147 | missense variant | A/T | snv | 4.0E-06 | 3 | ||
rs1057519701 | 1.000 | 0.080 | 4 | 54725978 | missense variant | G/A | snv | 1 | |||
rs1131692239 | 1.000 | 0.080 | 4 | 54727496 | inframe deletion | CTTATGATC/- | delins | 1 |