Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 13 | ||
rs3176867 | 1 | 100728649 | intron variant | C/A;T | snv | 1 | |||||
rs604723 | 1.000 | 0.040 | 11 | 100739815 | intron variant | T/C | snv | 0.78 | 9 | ||
rs10748798 | 10 | 100794914 | intron variant | C/T | snv | 0.91 | 1 | ||||
rs763802417 | 0.882 | 0.040 | X | 100862805 | missense variant | G/A | snv | 5.9E-06 | 5 | ||
rs1799889 | 0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv | 31 | |||
rs763351020 | 0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 | 35 | ||
rs9806366 | 15 | 101262752 | intergenic variant | C/T | snv | 0.24 | 1 | ||||
rs28628459 | 15 | 101272152 | intron variant | T/C | snv | 0.25 | 1 | ||||
rs12917258 | 15 | 101273134 | intron variant | C/G | snv | 0.19 | 1 | ||||
rs4965814 | 1.000 | 0.080 | 15 | 101273712 | intron variant | C/T | snv | 0.62 | 2 | ||
rs11053646 | 0.724 | 0.280 | 12 | 10160849 | missense variant | C/G | snv | 0.11 | 0.13 | 18 | |
rs1074703 | 8 | 101803258 | intron variant | C/A | snv | 0.63 | 1 | ||||
rs13127398 | 4 | 102000547 | intron variant | T/A | snv | 4.1E-02 | 1 | ||||
rs10409243 | 19 | 10222312 | 3 prime UTR variant | C/A;G;T | snv | 6 | |||||
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 | |||
rs5491 | 0.827 | 0.160 | 19 | 10274864 | missense variant | A/G;T | snv | 4.0E-06; 2.8E-02 | 6 | ||
rs281432 | 0.851 | 0.280 | 19 | 10279982 | intron variant | C/G | snv | 0.52 | 12 | ||
rs1799969 | 0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 | 38 | |
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
rs696217 | 0.662 | 0.640 | 3 | 10289773 | missense variant | G/T | snv | 8.8E-02 | 7.1E-02 | 32 | |
rs10903323 | 0.807 | 0.160 | 8 | 10292057 | intron variant | A/G | snv | 0.15 | 8 | ||
rs7681002 | 4 | 102974066 | intron variant | A/G | snv | 0.57 | 1 | ||||
rs2513993 | 11 | 103082247 | intron variant | A/G | snv | 0.32 | 1 |