| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2855268 | 0.882 | 0.040 | 2 | 222202200 | intron variant | C/G;T | snv | 0.11; 2.6E-05 | 3 | ||
| rs4636294 | 0.925 | 0.040 | 9 | 21747804 | intergenic variant | A/G | snv | 0.61 | 2 | ||
| rs7023954 | 0.925 | 0.040 | 9 | 21816759 | missense variant | G/A | snv | 0.40 | 0.42 | 2 | |
| rs7027989 | 0.925 | 0.120 | 9 | 21817755 | intron variant | A/G;T | snv | 2 | |||
| rs738322 | 0.925 | 0.040 | 22 | 38172999 | intron variant | A/G | snv | 0.52 | 2 | ||
| rs4608623 | 0.925 | 0.040 | 22 | 38201371 | non coding transcript exon variant | G/T | snv | 0.52 | 2 | ||
| rs10965135 | 1.000 | 0.040 | 9 | 21789581 | TF binding site variant | C/T | snv | 0.35 | 1 | ||
| rs4821767 | 1.000 | 0.040 | 22 | 38218122 | upstream gene variant | C/A | snv | 0.44 | 1 | ||
| rs10757236 | 1.000 | 0.040 | 9 | 21715891 | intergenic variant | G/C;T | snv | 1 | |||
| rs10811595 | 1.000 | 0.040 | 9 | 21715802 | intergenic variant | T/A;G | snv | 1 | |||
| rs6475555 | 1.000 | 0.040 | 9 | 21716998 | intergenic variant | A/C;G | snv | 0.58 | 1 | ||
| rs10811625 | 1.000 | 0.040 | 9 | 21826841 | intron variant | G/A;T | snv | 1 | |||
| rs10965144 | 1.000 | 0.040 | 9 | 21808914 | 5 prime UTR variant | C/T | snv | 0.36 | 1 | ||
| rs3900787 | 1.000 | 0.040 | 9 | 21828111 | intron variant | A/C;T | snv | 1 | |||
| rs3922992 | 1.000 | 0.040 | 9 | 21827407 | intron variant | A/G | snv | 0.34 | 1 | ||
| rs3927737 | 1.000 | 0.040 | 9 | 21827993 | intron variant | G/A;C | snv | 1 | |||
| rs132941 | 1.000 | 0.040 | 22 | 38149935 | non coding transcript exon variant | T/A;C | snv | 1 | |||
| rs84473 | 1.000 | 0.040 | 22 | 38161319 | intron variant | T/C | snv | 0.52 | 1 |