| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1003878 | 0.882 | 0.200 | 6 | 32332045 | stop gained | G/A | snv | 0.19 | 0.23 | 3 | |
| rs1003879 | 1.000 | 0.120 | 6 | 32331815 | intron variant | G/A | snv | 0.41 | 1 | ||
| rs1004819 | 0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 | 1 | ||
| rs1005133 | 1.000 | 0.120 | 22 | 19750832 | intergenic variant | C/T | snv | 0.20 | 1 | ||
| rs10088748 | 1.000 | 0.120 | 8 | 14611016 | intron variant | C/A | snv | 0.51 | 1 | ||
| rs10097964 | 1.000 | 0.120 | 8 | 21125392 | intron variant | G/A | snv | 2.6E-02 | 1 | ||
| rs10168266 | 0.776 | 0.400 | 2 | 191071078 | intron variant | C/T | snv | 0.19 | 4 | ||
| rs10174238 | 0.724 | 0.200 | 2 | 191108308 | intron variant | G/A | snv | 0.70 | 12 | ||
| rs10175798 | 1.000 | 0.120 | 2 | 30226728 | upstream gene variant | G/A | snv | 0.51 | 1 | ||
| rs10181656 | 0.763 | 0.360 | 2 | 191105153 | intron variant | G/C | snv | 0.79 | 1 | ||
| rs1018430 | 1.000 | 0.120 | 6 | 32313911 | intron variant | C/T | snv | 0.25 | 1 | ||
| rs1018431 | 1.000 | 0.120 | 6 | 32313899 | intron variant | G/A | snv | 0.25 | 1 | ||
| rs1018433 | 1.000 | 0.120 | 6 | 32313733 | intron variant | A/T | snv | 0.21 | 1 | ||
| rs1018434 | 1.000 | 0.120 | 6 | 32313583 | intron variant | T/C | snv | 0.21 | 1 | ||
| rs10203477 | 0.925 | 0.200 | 2 | 60877850 | intron variant | A/T | snv | 0.48 | 2 | ||
| rs10209110 | 1.000 | 0.120 | 2 | 100056230 | intron variant | C/T | snv | 0.47 | 1 | ||
| rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 16 | ||
| rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 4 | ||
| rs10275421 | 1.000 | 0.120 | 7 | 101299780 | non coding transcript exon variant | G/A | snv | 7.2E-02 | 1 | ||
| rs1033500 | 1.000 | 0.120 | 6 | 32339605 | missense variant | G/A | snv | 0.40 | 0.33 | 2 | |
| rs1034323 | 1.000 | 0.120 | 6 | 30400858 | intergenic variant | C/T | snv | 0.43 | 1 | ||
| rs1035142 | 0.807 | 0.200 | 2 | 201288355 | 3 prime UTR variant | T/C;G | snv | 0.54 | 1 | ||
| rs1041885 | 1.000 | 0.120 | 6 | 32445032 | 3 prime UTR variant | T/A | snv | 0.15 | 1 | ||
| rs1042127 | 0.925 | 0.120 | 6 | 31116393 | missense variant | A/C | snv | 0.21 | 0.17 | 1 | |
| rs1042337 | 1.000 | 0.120 | 6 | 32937204 | missense variant | G/A | snv | 0.78 | 0.80 | 1 |