Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10503929 | 0.925 | 0.040 | 8 | 32756465 | missense variant | T/C | snv | 0.13 | 0.13 | 3 | |
rs17512836 | 0.925 | 0.040 | 18 | 55527730 | intron variant | T/C | snv | 2.2E-02 | 3 | ||
rs4949526 | 1.000 | 0.040 | 1 | 29959372 | intergenic variant | T/C | snv | 0.54 | 3 | ||
rs1341402 | 1.000 | 0.040 | 13 | 105463160 | intron variant | T/C | snv | 0.16 | 2 | ||
rs1893490 | 1.000 | 0.040 | 18 | 50669431 | non coding transcript exon variant | T/C | snv | 0.48 | 2 | ||
rs2312147 | 1.000 | 0.040 | 2 | 57995793 | intron variant | T/C | snv | 0.70 | 2 | ||
rs3761554 | 1.000 | 0.040 | X | 123183391 | upstream gene variant | T/C | snv | 0.21 | 2 | ||
rs502434 | 1.000 | 0.040 | X | 123403426 | synonymous variant | T/C | snv | 0.59 | 2 | ||
rs6932590 | 1.000 | 0.040 | 6 | 27281152 | downstream gene variant | T/C | snv | 0.26 | 2 | ||
rs7248363 | 19 | 18357076 | intron variant | T/C | snv | 0.74 | 2 | ||||
rs769404 | 1.000 | 0.040 | 2 | 170822115 | synonymous variant | T/C | snv | 0.39 | 0.35 | 2 | |
rs2076369 | 0.925 | 0.040 | 22 | 38067645 | non coding transcript exon variant | T/A;G | snv | 3 | |||
rs35753505 | 0.827 | 0.080 | 8 | 31616625 | intergenic variant | T/A;C | snv | 6 | |||
rs3803300 | 0.827 | 0.120 | 14 | 104803442 | 3 prime UTR variant | T/A;C | snv | 6 | |||
rs1421292 | 0.925 | 0.040 | 13 | 105545886 | intergenic variant | T/A | snv | 0.39 | 3 | ||
rs12527359 | 6 | 89018502 | intergenic variant | T/A | snv | 0.23 | 2 | ||||
rs713729 | 1.000 | 0.040 | 22 | 38059462 | intron variant | T/A | snv | 0.20 | 2 | ||
rs4570625 | 0.724 | 0.200 | 12 | 71938143 | upstream gene variant | G/T | snv | 0.27 | 25 | ||
rs1625579 | 0.763 | 0.160 | 1 | 98037378 | intron variant | G/T | snv | 0.78 | 14 | ||
rs4996815 | 13 | 105999312 | intron variant | G/T | snv | 0.61 | 2 | ||||
rs1801028 | 0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 | 24 | |
rs135745 | 0.763 | 0.200 | 22 | 38287631 | downstream gene variant | G/C | snv | 0.48 | 13 | ||
rs2857766 | 0.882 | 0.120 | 6 | 29666226 | missense variant | G/C | snv | 0.22 | 0.19 | 4 | |
rs1806864 | 9 | 87416754 | regulatory region variant | G/C | snv | 7.4E-02 | 2 | ||||
rs7727102 | 5 | 4720472 | intron variant | G/C | snv | 0.32 | 2 |