| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10864728 | 1 | 230169168 | intron variant | A/G | snv | 0.50 | 3 | ||||
| rs12116643 | 1 | 197004053 | intron variant | T/C | snv | 0.19 | 3 | ||||
| rs191448950 | 1 | 55119171 | intron variant | G/A | snv | 6.4E-03 | 3 | ||||
| rs3737665 | 0.925 | 0.080 | 1 | 8970905 | missense variant | C/G;T | snv | 4.0E-06; 0.26 | 3 | ||
| rs3762318 | 0.925 | 0.040 | 1 | 67131436 | intron variant | G/A | snv | 0.83 | 3 | ||
| rs4657825 | 1.000 | 0.040 | 1 | 196615191 | intergenic variant | A/G;T | snv | 3 | |||
| rs10754199 | 1.000 | 0.040 | 1 | 196701709 | intron variant | A/G | snv | 0.64 | 2 | ||
| rs10801553 | 1.000 | 0.040 | 1 | 196686613 | intron variant | A/C | snv | 0.64 | 2 | ||
| rs10919543 | 1.000 | 0.080 | 1 | 161538827 | intron variant | A/G | snv | 0.28 | 2 | ||
| rs12038333 | 1.000 | 0.040 | 1 | 196703324 | intron variant | G/A | snv | 0.64 | 2 | ||
| rs12085435 | 1.000 | 0.040 | 1 | 56949637 | missense variant | G/A | snv | 4.8E-02 | 5.5E-02 | 2 | |
| rs12408663 | 1 | 19641564 | intron variant | T/C | snv | 0.19 | 2 | ||||
| rs1831282 | 1.000 | 0.040 | 1 | 196704863 | intron variant | A/C | snv | 0.62 | 2 | ||
| rs2099684 | 1.000 | 0.080 | 1 | 161530340 | intron variant | A/G | snv | 0.28 | 2 | ||
| rs2269233 | 1 | 63653675 | intron variant | T/C;G | snv | 2 | |||||
| rs2307246 | 1 | 19978364 | non coding transcript exon variant | G/A | snv | 0.18 | 0.18 | 2 | |||
| rs2808628 | 1 | 159706221 | upstream gene variant | G/A | snv | 0.31 | 2 | ||||
| rs35967351 | 1.000 | 0.080 | 1 | 160742014 | intron variant | A/T | snv | 0.26 | 2 | ||
| rs3820201 | 1 | 53115998 | non coding transcript exon variant | A/C;G;T | snv | 2 | |||||
| rs6685931 | 1.000 | 0.040 | 1 | 196898103 | intron variant | T/C | snv | 0.28 | 2 | ||
| rs6695321 | 1.000 | 0.040 | 1 | 196706731 | intron variant | A/G | snv | 0.36 | 2 | ||
| rs72660908 | 1 | 25257119 | intron variant | C/G | snv | 0.26 | 2 | ||||
| rs7519758 | 1.000 | 0.040 | 1 | 196856157 | intron variant | C/T | snv | 0.23 | 2 | ||
| rs7535475 | 1.000 | 0.080 | 1 | 161493797 | intergenic variant | C/A;T | snv | 2 | |||
| rs946261 | 1.000 | 0.080 | 1 | 203188745 | upstream gene variant | C/T | snv | 0.47 | 2 |