| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28601761 | 1.000 | 0.040 | 8 | 125487789 | intron variant | C/G | snv | 0.37 | 13 | ||
| rs715 | 1.000 | 0.040 | 2 | 210678331 | 3 prime UTR variant | T/C | snv | 0.28 | 13 | ||
| rs10857147 | 1.000 | 0.040 | 4 | 80259918 | intergenic variant | A/T | snv | 0.25 | 9 | ||
| rs13139571 | 1.000 | 0.040 | 4 | 155724361 | intron variant | C/A | snv | 0.22 | 9 | ||
| rs604723 | 1.000 | 0.040 | 11 | 100739815 | intron variant | T/C | snv | 0.78 | 9 | ||
| rs17608766 | 1.000 | 0.040 | 17 | 46935905 | 3 prime UTR variant | T/C | snv | 9.2E-02 | 8 | ||
| rs247616 | 1.000 | 0.040 | 16 | 56955678 | intergenic variant | C/T | snv | 0.29 | 8 | ||
| rs507666 | 1.000 | 0.040 | 9 | 133273983 | intron variant | A/G | snv | 8 | |||
| rs112635299 | 1.000 | 0.040 | 14 | 94371805 | downstream gene variant | G/T | snv | 1.3E-02 | 7 | ||
| rs5167 | 1.000 | 0.040 | 19 | 44945208 | missense variant | T/A;G | snv | 3.6E-05; 0.39 | 7 | ||
| rs12423664 | 1.000 | 0.040 | 12 | 132493308 | intron variant | G/A | snv | 0.10 | 6 | ||
| rs1800978 | 1.000 | 0.040 | 9 | 104903697 | 5 prime UTR variant | C/A;G;T | snv | 5.4E-06; 0.14 | 6 | ||
| rs7209400 | 1.000 | 0.040 | 17 | 49372695 | intron variant | C/T | snv | 0.47 | 6 | ||
| rs1250259 | 1.000 | 0.040 | 2 | 215435759 | missense variant | T/A | snv | 0.76 | 0.79 | 5 | |
| rs12801636 | 1.000 | 0.040 | 11 | 65623846 | intron variant | G/A | snv | 0.25 | 5 | ||
| rs15285 | 1.000 | 0.040 | 8 | 19967156 | 3 prime UTR variant | C/T | snv | 0.36 | 5 | ||
| rs2865531 | 1.000 | 0.040 | 16 | 75356418 | intron variant | T/A | snv | 0.52 | 5 | ||
| rs5883 | 1.000 | 0.040 | 16 | 56973441 | synonymous variant | C/T | snv | 5.1E-02 | 6.6E-02 | 5 | |
| rs611917 | 1.000 | 0.040 | 1 | 109272630 | non coding transcript exon variant | A/G | snv | 0.28 | 0.32 | 5 | |
| rs895953 | 1.000 | 0.040 | 12 | 121811142 | intron variant | G/T | snv | 0.76 | 5 | ||
| rs1250229 | 1.000 | 0.040 | 2 | 215439661 | upstream gene variant | T/C | snv | 0.77 | 4 | ||
| rs16844401 | 1.000 | 0.040 | 4 | 3447925 | missense variant | G/A;T | snv | 7.5E-02; 8.3E-06 | 4 | ||
| rs1800787 | 1.000 | 0.040 | 4 | 154562863 | upstream gene variant | C/T | snv | 0.17 | 4 | ||
| rs1800789 | 1.000 | 0.040 | 4 | 154561591 | upstream gene variant | G/A | snv | 0.17 | 4 | ||
| rs2281719 | 1.000 | 0.040 | 1 | 230161913 | intron variant | C/T | snv | 0.45 | 4 |