| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs116088953 | 1.000 | 0.080 | 6 | 31475005 | intron variant | G/A | snv | 1 | |||
| rs6659932 | 0.827 | 0.240 | 1 | 67336688 | intron variant | A/C | snv | 0.81 | 4 | ||
| rs10954214 | 0.851 | 0.160 | 7 | 128949579 | 3 prime UTR variant | C/T | snv | 0.64 | 4 | ||
| rs2422345 | 0.851 | 0.160 | 1 | 173368608 | upstream gene variant | G/A | snv | 0.63 | 4 | ||
| rs3130614 | 1.000 | 0.080 | 6 | 31508681 | intron variant | T/A | snv | 7.3E-02 | 1 | ||
| rs114771815 | 1.000 | 0.080 | 6 | 31484059 | intron variant | T/C | snv | 1 | |||
| rs116662199 | 1.000 | 0.080 | 6 | 31481199 | non coding transcript exon variant | C/A | snv | 1 | |||
| rs17849502 | 0.827 | 0.240 | 1 | 183563445 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 3.4E-02 | 5 | ||
| rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 25 | ||
| rs76246107 | 0.851 | 0.160 | 19 | 49618017 | intron variant | G/A | snv | 7.7E-02 | 4 | ||
| rs11066301 | 0.827 | 0.200 | 12 | 112433568 | intron variant | A/G | snv | 0.30 | 7 | ||
| rs10174238 | 0.724 | 0.200 | 2 | 191108308 | intron variant | G/A | snv | 0.70 | 12 | ||
| rs13389408 | 0.851 | 0.160 | 2 | 191068557 | 3 prime UTR variant | T/C | snv | 7.4E-02 | 4 | ||
| rs4958880 | 0.851 | 0.160 | 5 | 151058916 | intron variant | C/A;G | snv | 4 | |||
| rs13238352 | 0.827 | 0.240 | 7 | 129007888 | intron variant | C/T | snv | 9.1E-02 | 4 | ||
| rs11085725 | 0.851 | 0.160 | 19 | 10351837 | intron variant | C/T | snv | 0.24 | 4 |