Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13415583 | 1.000 | 0.120 | 2 | 100147625 | intron variant | T/G | snv | 0.37 | 1 | ||
rs941576 | 1.000 | 0.120 | 14 | 100839708 | intron variant | A/G | snv | 0.45 | 1 | ||
rs56994090 | 1.000 | 0.120 | 14 | 100840110 | intron variant | T/A;C | snv | 1 | |||
rs3733197 | 0.742 | 0.320 | 4 | 101918130 | missense variant | G/A | snv | 0.31 | 0.30 | 13 | |
rs879228335 | 1.000 | 0.120 | 14 | 102229329 | missense variant | T/C | snv | 1 | |||
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs917997 | 0.701 | 0.480 | 2 | 102454108 | downstream gene variant | T/A;C | snv | 20 | |||
rs2075184 | 0.724 | 0.240 | 2 | 102464132 | intergenic variant | T/C | snv | 0.78 | 14 | ||
rs281432 | 0.851 | 0.280 | 19 | 10279982 | intron variant | C/G | snv | 0.52 | 12 | ||
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
rs34536443 | 0.667 | 0.400 | 19 | 10352442 | missense variant | G/C | snv | 2.7E-02 | 2.8E-02 | 25 | |
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 12 | ||
rs2304256 | 0.732 | 0.360 | 19 | 10364976 | missense variant | C/A | snv | 0.27 | 0.23 | 13 | |
rs28641753 | 0.925 | 0.160 | 3 | 104256574 | intergenic variant | C/T | snv | 4.5E-02 | 2 | ||
rs62131887 | 0.724 | 0.240 | 19 | 10476920 | intergenic variant | C/T | snv | 0.37 | 14 | ||
rs9810233 | 0.925 | 0.200 | 3 | 105292046 | intergenic variant | A/G | snv | 0.25 | 2 | ||
rs1223438908 | 1.000 | 0.120 | 3 | 105681480 | missense variant | T/G | snv | 4.0E-06 | 2 | ||
rs752455542 | 1.000 | 0.120 | 3 | 105681740 | missense variant | T/G | snv | 4.0E-06 | 2 | ||
rs3772534 | 1.000 | 0.120 | 3 | 105702190 | synonymous variant | C/T | snv | 3.1E-02 | 2.0E-02 | 1 | |
rs1950942 | 1.000 | 0.120 | 14 | 105861856 | upstream gene variant | A/C;G | snv | 1 | |||
rs1358030 | 0.925 | 0.120 | 10 | 106363841 | intergenic variant | G/A | snv | 0.57 | 2 | ||
rs11839053 | 0.724 | 0.240 | 13 | 106410694 | intergenic variant | T/C | snv | 7.0E-02 | 14 | ||
rs1460002897 | 1.000 | 0.120 | 7 | 107793769 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs11074932 | 1.000 | 0.120 | 16 | 10874479 | intron variant | T/A;C | snv | 1 | |||
rs3087456 | 0.742 | 0.480 | 16 | 10877045 | intron variant | G/A | snv | 0.53 | 14 |