Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs28362491 | 0.592 | 0.720 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 56 | |||
rs72696119 | 0.925 | 0.120 | 4 | 102501347 | 5 prime UTR variant | C/G | snv | 0.43 | 3 | ||
rs35866072 | 0.716 | 0.360 | 11 | 102713373 | missense variant | T/G | snv | 6.0E-02 | 9.8E-02 | 17 | |
rs34009635 | 0.716 | 0.360 | 11 | 102713445 | missense variant | A/G | snv | 2.5E-03 | 6.2E-04 | 17 | |
rs28903081 | 0.851 | 0.200 | 14 | 103698934 | missense variant | C/A;T | snv | 4.5E-06; 4.3E-04 | 5 | ||
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
rs511044 | 0.925 | 0.120 | 11 | 105024783 | upstream gene variant | T/C | snv | 3 | |||
rs221636 | 1.000 | 0.120 | 6 | 105082089 | 3 prime UTR variant | T/A | snv | 0.82 | 2 | ||
rs189037 | 0.689 | 0.400 | 11 | 108223106 | 5 prime UTR variant | G/A | snv | 0.49 | 22 | ||
rs2070894 | 0.851 | 0.160 | 11 | 111910113 | 3 prime UTR variant | G/A | snv | 0.27 | 5 | ||
rs2228387 | 0.851 | 0.160 | 11 | 111911560 | synonymous variant | C/G;T | snv | 1.5E-02 | 5 | ||
rs14133 | 0.807 | 0.200 | 11 | 111911973 | 5 prime UTR variant | G/C | snv | 0.27 | 7 | ||
rs7085532 | 1.000 | 0.080 | 10 | 113099704 | intron variant | G/A | snv | 0.72 | 2 | ||
rs2227310 | 0.807 | 0.160 | 10 | 113729393 | missense variant | C/G | snv | 0.26 | 0.23 | 9 | |
rs3807987 | 0.732 | 0.280 | 7 | 116539780 | intron variant | G/A | snv | 7.6E-02 | 17 | ||
rs7804372 | 0.716 | 0.320 | 7 | 116554174 | intron variant | T/A | snv | 0.27 | 19 | ||
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 93 | |
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
rs8898 | 0.925 | 0.120 | 8 | 11845033 | 3 prime UTR variant | T/C | snv | 0.37 | 5 | ||
rs13332 | 0.925 | 0.120 | 8 | 11849072 | synonymous variant | T/C;G | snv | 3.5E-02; 0.56 | 6 | ||
rs12338 | 0.807 | 0.200 | 8 | 11853379 | missense variant | G/A;C;T | snv | 8.0E-06; 0.38; 2.4E-05 | 10 | ||
rs9879992 | 0.882 | 0.120 | 3 | 119993874 | intron variant | A/G | snv | 0.28 | 4 |