| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17849502 | 0.827 | 0.240 | 1 | 183563445 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 3.4E-02 | 5 | ||
| rs2431098 | 0.827 | 0.240 | 5 | 160460329 | intron variant | A/G;T | snv | 5 | |||
| rs35677470 | 0.807 | 0.160 | 3 | 58197909 | missense variant | G/A;C | snv | 4.8E-02; 4.0E-06 | 5 | ||
| rs35929052 | 0.827 | 0.160 | 16 | 85960878 | downstream gene variant | C/G;T | snv | 5 | |||
| rs4958880 | 0.851 | 0.160 | 5 | 151058916 | intron variant | C/A;G | snv | 4 | |||
| rs5754467 | 0.851 | 0.160 | 22 | 21630805 | upstream gene variant | A/G;T | snv | 4 | |||
| rs58721818 | 0.851 | 0.160 | 6 | 137922602 | regulatory region variant | C/G;T | snv | 4 | |||
| rs114012716 | 1.000 | 0.080 | 6 | 31466589 | non coding transcript exon variant | G/A | snv | 1 | |||
| rs114042950 | 1.000 | 0.080 | 6 | 32699098 | intergenic variant | A/G | snv | 1 | |||
| rs114050967 | 1.000 | 0.080 | 6 | 31537703 | intron variant | A/G | snv | 1 | |||
| rs114388793 | 1.000 | 0.080 | 6 | 32699566 | intergenic variant | A/T | snv | 1 | |||
| rs114771815 | 1.000 | 0.080 | 6 | 31484059 | intron variant | T/C | snv | 1 | |||
| rs115146037 | 1.000 | 0.080 | 6 | 31466554 | non coding transcript exon variant | A/T | 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 | |||
| rs193107685 | 0.851 | 0.160 | 7 | 74123572 | downstream gene variant | T/C | snv | 1.0E-02 | 4 | ||
| rs112846137 | 0.851 | 0.160 | 3 | 160595133 | intergenic variant | G/T | snv | 5.3E-02 | 4 | ||
| rs3129843 | 0.827 | 0.160 | 6 | 32427949 | intergenic variant | A/G | snv | 6.3E-02 | 4 | ||
| rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 25 | ||
| rs3130614 | 1.000 | 0.080 | 6 | 31508681 | intron variant | T/A | snv | 7.3E-02 | 1 | ||
| rs13389408 | 0.851 | 0.160 | 2 | 191068557 | 3 prime UTR variant | T/C | snv | 7.4E-02 | 4 | ||
| rs76246107 | 0.851 | 0.160 | 19 | 49618017 | intron variant | G/A | snv | 7.7E-02 | 4 | ||
| rs13238352 | 0.827 | 0.240 | 7 | 129007888 | intron variant | C/T | snv | 9.1E-02 | 4 | ||
| rs9267488 | 1.000 | 0.080 | 6 | 31546470 | splice region variant | A/G | snv | 8.1E-02 | 9.9E-02 | 1 |