| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10212536 | 1.000 | 0.160 | 3 | 41785534 | intron variant | A/C;G | snv | 1 | |||
| rs1025646 | 1.000 | 0.160 | 3 | 41712930 | intron variant | A/T | snv | 0.26 | 1 | ||
| rs1034447 | 1.000 | 0.160 | 6 | 164192425 | intergenic variant | C/T | snv | 0.24 | 1 | ||
| rs10452020 | 1.000 | 0.160 | 3 | 41774459 | intron variant | A/C;G | snv | 1 | |||
| rs10452022 | 1.000 | 0.160 | 3 | 41774550 | intron variant | G/A;C | snv | 1 | |||
| rs1045433 | 1.000 | 0.160 | 3 | 3149742 | non coding transcript exon variant | T/C | snv | 0.15 | 1 | ||
| rs10485986 | 1.000 | 0.160 | 7 | 21867059 | intron variant | C/T | snv | 0.32 | 1 | ||
| rs1049633 | 1.000 | 0.160 | 6 | 30899750 | 3 prime UTR variant | G/A | snv | 7.6E-02 | 1 | ||
| rs10509328 | 1.000 | 0.160 | 10 | 71007652 | intron variant | T/A;C | snv | 1 | |||
| rs10510729 | 1.000 | 0.160 | 3 | 41790506 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs10510731 | 1.000 | 0.160 | 3 | 41811818 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs10510732 | 1.000 | 0.160 | 3 | 41965847 | upstream gene variant | G/A | snv | 0.12 | 1 | ||
| rs10510733 | 1.000 | 0.160 | 3 | 41967700 | intergenic variant | T/C | snv | 0.13 | 1 | ||
| rs10865914 | 1.000 | 0.160 | 3 | 41878007 | intron variant | C/A;G;T | snv | 1 | |||
| rs10936600 | 1.000 | 0.160 | 3 | 169796797 | missense variant | A/T | snv | 0.29 | 0.21 | 1 | |
| rs10936603 | 1.000 | 0.160 | 3 | 169827864 | intron variant | G/A;T | snv | 1 | |||
| rs11064392 | 1.000 | 0.160 | 12 | 6789226 | intron variant | A/G | snv | 0.14 | 1 | ||
| rs11086029 | 1.000 | 0.160 | 19 | 16327850 | 3 prime UTR variant | T/A | snv | 0.78 | 1 | ||
| rs11129932 | 1.000 | 0.160 | 3 | 41797275 | intron variant | C/A | snv | 0.12 | 1 | ||
| rs11129935 | 1.000 | 0.160 | 3 | 41943711 | intron variant | A/C | snv | 0.13 | 1 | ||
| rs111304140 | 1.000 | 0.160 | 3 | 41765000 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs111419796 | 1.000 | 0.160 | 3 | 41935476 | intron variant | G/A;C | snv | 1 | |||
| rs111465678 | 1.000 | 0.160 | 3 | 41822913 | intron variant | C/A;T | snv | 1 | |||
| rs111634789 | 1.000 | 0.160 | 3 | 41829864 | intron variant | T/C;G | snv | 1 | |||
| rs111708447 | 1.000 | 0.160 | 3 | 41768091 | intron variant | G/A | snv | 0.12 | 1 |