Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17759659 | 0.851 | 0.120 | 18 | 63291411 | intron variant | A/G | snv | 0.31 | 4 | ||
rs12478601 | 0.851 | 0.200 | 2 | 43494369 | intron variant | C/T | snv | 0.61 | 5 | ||
rs4385527 | 0.827 | 0.280 | 9 | 94886305 | intron variant | G/A | snv | 0.31 | 6 | ||
rs10818854 | 0.851 | 0.200 | 9 | 123684499 | intron variant | G/A | snv | 5.7E-02 | 6 | ||
rs1057518903 | 0.882 | 0.160 | 11 | 64807890 | splice region variant | C/- | delins | 6 | |||
rs13429458 | 0.827 | 0.200 | 2 | 43411699 | intron variant | A/C | snv | 0.14 | 6 | ||
rs2059807 | 0.851 | 0.200 | 19 | 7166098 | intron variant | A/G;T | snv | 7 | |||
rs13405728 | 0.790 | 0.200 | 2 | 48751020 | intron variant | A/G | snv | 0.15 | 8 | ||
rs2234767 | 0.649 | 0.280 | 10 | 88989499 | intron variant | G/A;T | snv | 0.15 | 30 | ||
rs121913364 | 0.641 | 0.520 | 7 | 140753334 | missense variant | T/C;G | snv | 4.0E-06 | 34 | ||
rs5443 | 0.532 | 0.760 | 12 | 6845711 | synonymous variant | C/T | snv | 0.36 | 0.44 | 106 | |
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 |