Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs705699 | 0.882 | 0.160 | 12 | 55991020 | non coding transcript exon variant | G/A | snv | 0.40 | 5 | ||
rs10414065 | 0.882 | 0.080 | 19 | 33230549 | upstream gene variant | C/T | snv | 5.5E-02 | 4 | ||
rs12413578 | 0.882 | 0.160 | 10 | 9007290 | intergenic variant | C/G;T | snv | 4 | |||
rs17144046 | 0.882 | 0.120 | 10 | 8564051 | intergenic variant | A/G | snv | 0.28 | 4 | ||
rs17454584 | 0.851 | 0.080 | 4 | 122432277 | downstream gene variant | A/G | snv | 0.17 | 4 | ||
rs6594499 | 0.882 | 0.120 | 5 | 111134439 | downstream gene variant | C/A | snv | 0.56 | 4 | ||
rs61894547 | 0.882 | 0.160 | 11 | 76537586 | intron variant | C/T | snv | 3.1E-02 | 4 | ||
rs2070901 | 0.882 | 0.120 | 1 | 161215268 | non coding transcript exon variant | G/T | snv | 0.32 | 4 | ||
rs2305480 | 0.763 | 0.280 | 17 | 39905943 | missense variant | G/A | snv | 0.40 | 0.35 | 4 | |
rs9272346 | 0.790 | 0.320 | 6 | 32636595 | intron variant | G/A | snv | 0.54 | 4 | ||
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 4 | |
rs72823641 | 0.882 | 0.080 | 2 | 102319699 | intron variant | T/A;C | snv | 4 | |||
rs12722502 | 0.882 | 0.080 | 10 | 6051176 | intron variant | C/T | snv | 7.8E-03 | 4 | ||
rs3749833 | 0.925 | 0.080 | 5 | 132463934 | non coding transcript exon variant | T/C | snv | 0.23 | 4 | ||
rs9391997 | 0.851 | 0.160 | 6 | 409119 | 3 prime UTR variant | A/G | snv | 0.38 | 4 | ||
rs12123821 | 0.925 | 0.080 | 1 | 152206676 | intron variant | C/T | snv | 2.9E-02 | 4 | ||
rs143326447 | 0.925 | 0.080 | 2 | 111511155 | intron variant | T/C | snv | 0.11 | 4 | ||
rs11071559 | 0.925 | 0.080 | 15 | 60777789 | intron variant | C/T | snv | 0.23 | 4 | ||
rs3122929 | 0.882 | 0.080 | 12 | 57115319 | intron variant | C/T | snv | 0.33 | 4 | ||
rs1295685 | 0.790 | 0.160 | 5 | 132660753 | 3 prime UTR variant | A/G | snv | 0.81 | 4 | ||
rs4574025 | 0.882 | 0.160 | 18 | 62342581 | intron variant | C/T | snv | 0.55 | 4 | ||
rs10036789 | 1.000 | 0.080 | 5 | 72400091 | regulatory region variant | C/A;G | snv | 3 | |||
rs1102705 | 0.925 | 0.080 | 1 | 172731728 | intergenic variant | G/A | snv | 0.93 | 3 | ||
rs13277355 | 0.882 | 0.120 | 8 | 127765473 | intergenic variant | A/G | snv | 0.71 | 3 | ||
rs1775554 | 0.882 | 0.080 | 10 | 9012377 | intergenic variant | A/C | snv | 0.35 | 3 |