| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1001007 | 0.827 | 0.120 | 3 | 46387167 | intron variant | A/G;T | snv | 5 | |||
| rs10019009 | 0.851 | 0.080 | 4 | 87661983 | missense variant | A/G;T | snv | 4.0E-06; 0.29 | 4 | ||
| rs1004189 | 1.000 | 0.040 | 2 | 208349547 | intron variant | T/G | snv | 1 | |||
| rs1004234 | 0.827 | 0.120 | 5 | 132421409 | intron variant | A/G;T | snv | 5 | |||
| rs10045403 | 0.882 | 0.040 | 5 | 96812030 | upstream gene variant | A/G | snv | 0.23 | 3 | ||
| rs1004819 | 0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 | 9 | ||
| rs10050860 | 0.882 | 0.240 | 5 | 96786506 | missense variant | C/T | snv | 0.15 | 0.16 | 4 | |
| rs10065172 | 0.790 | 0.200 | 5 | 150848436 | synonymous variant | C/T | snv | 0.17 | 0.21 | 8 | |
| rs10094579 | 0.807 | 0.280 | 8 | 89837077 | downstream gene variant | C/A | snv | 0.18 | 6 | ||
| rs1009759 | 1.000 | 0.040 | 9 | 5556786 | intron variant | A/C;G | snv | 1 | |||
| rs1013210 | 1.000 | 0.040 | 8 | 24259209 | intergenic variant | G/A;C;T | snv | 1 | |||
| rs10204525 | 0.701 | 0.440 | 2 | 241850169 | 3 prime UTR variant | C/T | snv | 0.21 | 20 | ||
| rs10208769 | 1.000 | 0.040 | 2 | 61378479 | intron variant | T/A | snv | 0.48 | 1 | ||
| rs1024446168 | 1.000 | 0.040 | X | 47583421 | synonymous variant | C/A | snv | 1.7E-05 | 1 | ||
| rs10280089 | 1.000 | 0.040 | 7 | 38667217 | intergenic variant | C/A;T | snv | 1 | |||
| rs10440635 | 1.000 | 0.040 | 5 | 40490688 | intron variant | G/A | snv | 0.56 | 2 | ||
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs1048274 | 1.000 | 0.040 | 9 | 6256292 | 3 prime UTR variant | G/A | snv | 0.35 | 1 | ||
| rs10489630 | 0.925 | 0.040 | 1 | 67196939 | intron variant | A/C;T | snv | 2 | |||
| rs10494829 | 1.000 | 0.040 | 1 | 200968901 | downstream gene variant | G/A | snv | 0.26 | 1 | ||
| rs10499194 | 0.752 | 0.400 | 6 | 137681500 | intron variant | C/T | snv | 0.24 | 10 | ||
| rs1050501 | 0.732 | 0.440 | 1 | 161674008 | missense variant | T/C | snv | 0.16 | 0.19 | 15 | |
| rs10510607 | 0.827 | 0.120 | 3 | 28244770 | intron variant | C/T | snv | 0.15 | 5 | ||
| rs1053005 | 0.763 | 0.360 | 17 | 42313892 | 3 prime UTR variant | T/C | snv | 0.25 | 10 | ||
| rs1055234 | 1.000 | 0.040 | 19 | 54154264 | 3 prime UTR variant | G/A;C;T | snv | 1 |