| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10019835 | 1.000 | 0.120 | 4 | 155712034 | intron variant | T/A;C | snv | 1 | |||
| rs10047560 | 1.000 | 0.120 | 12 | 20452282 | intron variant | A/G | snv | 0.86 | 1 | ||
| rs10255208 | 0.925 | 0.160 | 7 | 36819038 | non coding transcript exon variant | A/G | snv | 0.46 | 2 | ||
| rs1034589 | 1.000 | 0.120 | 22 | 31183247 | intron variant | C/T | snv | 0.79 | 1 | ||
| rs1044498 | 0.752 | 0.360 | 6 | 131851228 | missense variant | A/C;G | snv | 0.19 | 15 | ||
| rs1049353 | 0.630 | 0.600 | 6 | 88143916 | synonymous variant | C/T | snv | 0.21 | 0.20 | 42 | |
| rs1056534 | 0.882 | 0.200 | 17 | 82750725 | synonymous variant | C/A;G;T | snv | 0.62 | 5 | ||
| rs1063537 | 0.807 | 0.320 | 3 | 186856286 | 3 prime UTR variant | C/T | snv | 9.6E-02 | 6 | ||
| rs10770125 | 0.882 | 0.200 | 11 | 2147784 | missense variant | A/G | snv | 0.49 | 0.40 | 4 | |
| rs10811661 | 0.724 | 0.400 | 9 | 22134095 | intergenic variant | T/C | snv | 0.14 | 22 | ||
| rs10823108 | 0.925 | 0.160 | 10 | 67900736 | intron variant | G/A | snv | 7.1E-02 | 2 | ||
| rs10868025 | 1.000 | 0.120 | 9 | 83549261 | intergenic variant | A/G | snv | 0.30 | 1 | ||
| rs10951509 | 1.000 | 0.120 | 7 | 37173878 | intron variant | G/A;C | snv | 1 | |||
| rs10952362 | 1.000 | 0.120 | 7 | 152565713 | regulatory region variant | T/C | snv | 0.25 | 1 | ||
| rs11107616 | 1.000 | 0.120 | 12 | 77971000 | intron variant | T/G | snv | 0.13 | 1 | ||
| rs11130362 | 1.000 | 0.120 | 3 | 53231750 | non coding transcript exon variant | C/T | snv | 0.24 | 1 | ||
| rs1129456 | 1.000 | 0.120 | 15 | 32734466 | 3 prime UTR variant | A/T | snv | 0.19 | 1 | ||
| rs1136410 | 0.559 | 0.760 | 1 | 226367601 | missense variant | A/G | snv | 0.21 | 0.15 | 70 | |
| rs1137933 | 0.882 | 0.160 | 17 | 27778906 | synonymous variant | G/A | snv | 0.20 | 0.21 | 4 | |
| rs1143770 | 0.882 | 0.200 | 11 | 122146890 | intron variant | C/T | snv | 0.53 | 4 | ||
| rs11538209 | 1.000 | 0.120 | 4 | 73404356 | missense variant | T/C | snv | 2 | |||
| rs11549465 | 0.597 | 0.680 | 14 | 61740839 | missense variant | C/T | snv | 8.8E-02 | 7.7E-02 | 55 | |
| rs1157043147 | 1.000 | 0.120 | 17 | 63477150 | missense variant | T/C | snv | 2.8E-05 | 1 | ||
| rs11643718 | 0.807 | 0.240 | 16 | 56899607 | missense variant | G/A | snv | 0.11 | 8.4E-02 | 10 | |
| rs11645214 | 1.000 | 0.120 | 16 | 70575084 | 3 prime UTR variant | A/G | snv | 0.39 | 1 |