Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 7 | ||
rs17712208 | 1 | 213977102 | intron variant | T/A | snv | 2.1E-02 | 2 | ||||
rs340878 | 1 | 213983706 | intron variant | G/C | snv | 0.63 | 2 | ||||
rs17407594 | 1 | 65704679 | intron variant | G/A;T | snv | 1 | |||||
rs79687284 | 1 | 213977478 | intron variant | G/A;C;T | snv | 1 | |||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs560887 | 0.827 | 0.120 | 2 | 168906638 | intron variant | T/C | snv | 0.79 | 0.80 | 18 | |
rs2068834 | 0.925 | 0.120 | 2 | 27616672 | intron variant | T/C | snv | 0.28 | 10 | ||
rs1919128 | 0.882 | 0.120 | 2 | 27578892 | missense variant | A/G | snv | 0.30 | 0.24 | 8 | |
rs3749147 | 0.882 | 0.120 | 2 | 27629051 | missense variant | G/A | snv | 0.23 | 0.20 | 8 | |
rs13431652 | 0.925 | 0.080 | 2 | 168896905 | intron variant | T/C | snv | 0.24 | 5 | ||
rs13023194 | 0.925 | 0.120 | 2 | 27744393 | intergenic variant | G/A;C | snv | 4 | |||
rs13404446 | 0.925 | 0.120 | 2 | 27296386 | intron variant | G/A | snv | 0.42 | 4 | ||
rs1395 | 0.882 | 0.200 | 2 | 27201768 | missense variant | G/A | snv | 0.62 | 0.55 | 4 | |
rs2305929 | 1.000 | 0.040 | 2 | 27891044 | intron variant | A/G | snv | 0.14 | 4 | ||
rs4665965 | 0.925 | 0.120 | 2 | 27313513 | intron variant | T/A;C | snv | 4 | |||
rs780110 | 0.925 | 0.120 | 2 | 27462521 | intron variant | G/A | snv | 0.56 | 4 | ||
rs853789 | 2 | 168944978 | intron variant | A/G;T | snv | 0.75 | 4 | ||||
rs1371614 | 2 | 26930006 | intron variant | C/T | snv | 0.29 | 3 | ||||
rs2232326 | 2 | 168907981 | missense variant | T/C | snv | 5.1E-03 | 3.3E-03 | 3 | |||
rs3736594 | 2 | 27772914 | intron variant | A/C | snv | 0.62 | 3 | ||||
rs1124649 | 2 | 27037601 | missense variant | G/A | snv | 0.32 | 0.35 | 2 | |||
rs11891554 | 2 | 27390750 | intron variant | G/A;T | snv | 7.1E-02 | 2 | ||||
rs16856247 | 2 | 168927903 | intron variant | C/T | snv | 6.6E-02 | 2 |