| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs769178 | 1.000 | 0.040 | 6 | 31579737 | downstream gene variant | G/T | snv | 8.3E-02 | 2 | ||
| rs7857730 | 0.925 | 0.040 | 9 | 5084049 | intron variant | G/A;T | snv | 0.63 | 2 | ||
| rs9276615 | 0.925 | 0.040 | 6 | 32775440 | intergenic variant | C/T | snv | 0.70 | 2 | ||
| rs9438876 | 1.000 | 0.040 | 1 | 24914625 | intron variant | A/G | snv | 0.53 | 2 | ||
| rs1004189 | 1.000 | 0.040 | 2 | 208349547 | intron variant | T/G | snv | 1 | |||
| 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 | |||
| 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 | |||
| rs1048274 | 1.000 | 0.040 | 9 | 6256292 | 3 prime UTR variant | G/A | snv | 0.35 | 1 | ||
| rs10494829 | 1.000 | 0.040 | 1 | 200968901 | downstream gene variant | G/A | snv | 0.26 | 1 | ||
| rs1055234 | 1.000 | 0.040 | 19 | 54154264 | 3 prime UTR variant | G/A;C;T | snv | 1 | |||
| rs10781500 | 1.000 | 0.040 | 9 | 136374886 | upstream gene variant | C/G;T | snv | 1 | |||
| rs11062357 | 1.000 | 0.040 | 12 | 312228 | intron variant | T/C | snv | 0.33 | 1 | ||
| rs11062385 | 1.000 | 0.040 | 12 | 318409 | missense variant | A/C;G | snv | 1.2E-05; 0.31 | 1 | ||
| rs11145835 | 1.000 | 0.040 | 9 | 136390000 | intron variant | A/G | snv | 0.10 | 1 | ||
| rs11187265 | 1.000 | 0.040 | 10 | 93064409 | missense variant | G/A | snv | 0.10 | 8.8E-02 | 1 | |
| rs11249215 | 1.000 | 0.040 | 1 | 24970693 | non coding transcript exon variant | G/A | snv | 0.44 | 1 | ||
| rs1128905 | 1.000 | 0.040 | 9 | 136359387 | 3 prime UTR variant | T/C | snv | 0.46 | 1 | ||
| rs11428092 | 1.000 | 0.040 | 2 | 61301164 | intron variant | -/A | delins | 0.34 | 1 | ||
| rs11547635 | 1.000 | 0.040 | 22 | 32857305 | synonymous variant | C/A;T | snv | 0.11 | 1 | ||
| rs11578380 | 1.000 | 0.040 | 1 | 67295682 | intergenic variant | G/A;C | snv | 1 | |||
| rs1160489801 | 1.000 | 0.040 | 2 | 112918672 | missense variant | G/A | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs11742270 | 1.000 | 0.040 | 5 | 35881341 | downstream gene variant | G/A | snv | 0.20 | 1 |