Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11085725 | 0.851 | 0.160 | 19 | 10351837 | intron variant | C/T | snv | 0.24 | 4 | ||
rs802791 | 0.851 | 0.160 | 6 | 106121395 | intron variant | T/C | snv | 0.75 | 4 | ||
rs11066301 | 0.827 | 0.200 | 12 | 112433568 | intron variant | A/G | snv | 0.30 | 7 | ||
rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 25 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 34 | |
rs1217393 | 0.851 | 0.160 | 1 | 113891324 | intron variant | G/A | snv | 0.42 | 4 | ||
rs2736337 | 0.827 | 0.240 | 8 | 11484371 | upstream gene variant | T/C | snv | 0.26 | 4 | ||
rs2736340 | 0.683 | 0.480 | 8 | 11486464 | upstream gene variant | C/T | snv | 0.25 | 4 | ||
rs10954214 | 0.851 | 0.160 | 7 | 128949579 | 3 prime UTR variant | C/T | snv | 0.64 | 4 | ||
rs13238352 | 0.827 | 0.240 | 7 | 129007888 | intron variant | C/T | snv | 9.1E-02 | 4 | ||
rs58721818 | 0.851 | 0.160 | 6 | 137922602 | regulatory region variant | C/G;T | snv | 4 | |||
rs4958880 | 0.851 | 0.160 | 5 | 151058916 | intron variant | C/A;G | snv | 4 | |||
rs2431098 | 0.827 | 0.240 | 5 | 160460329 | intron variant | A/G;T | snv | 5 | |||
rs112846137 | 0.851 | 0.160 | 3 | 160595133 | intergenic variant | G/T | snv | 5.3E-02 | 4 | ||
rs2422345 | 0.851 | 0.160 | 1 | 173368608 | upstream gene variant | G/A | snv | 0.63 | 4 | ||
rs17849502 | 0.827 | 0.240 | 1 | 183563445 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 3.4E-02 | 5 | ||
rs744600 | 0.851 | 0.160 | 2 | 190700031 | intron variant | G/T | snv | 0.60 | 4 | ||
rs13389408 | 0.851 | 0.160 | 2 | 191068557 | 3 prime UTR variant | T/C | snv | 7.4E-02 | 4 | ||
rs10174238 | 0.724 | 0.200 | 2 | 191108308 | intron variant | G/A | snv | 0.70 | 12 | ||
rs5754467 | 0.851 | 0.160 | 22 | 21630805 | upstream gene variant | A/G;T | snv | 4 | |||
rs115146037 | 1.000 | 0.080 | 6 | 31466554 | non coding transcript exon variant | A/T | snv | 1 | |||
rs114012716 | 1.000 | 0.080 | 6 | 31466589 | non coding transcript exon variant | G/A | snv | 1 | |||
rs115902351 | 1.000 | 0.080 | 6 | 31466844 | non coding transcript exon variant | A/G | snv | 1 | |||
rs116088953 | 1.000 | 0.080 | 6 | 31475005 | intron variant | G/A | snv | 1 | |||
rs116662199 | 1.000 | 0.080 | 6 | 31481199 | non coding transcript exon variant | C/A | snv | 1 |