| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057519807 | 1.000 | 0.040 | 19 | 4110586 | missense variant | A/T | snv | 1 | |||
| rs1057519809 | 1.000 | 0.040 | 19 | 4117586 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs1057519810 | 1.000 | 0.040 | 19 | 4117619 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
| rs1057519811 | 1.000 | 0.040 | 4 | 54274916 | missense variant | C/T | snv | 1 | |||
| rs1057519812 | 1.000 | 0.040 | 4 | 54277977 | missense variant | T/C | snv | 1 | |||
| rs1057519813 | 1.000 | 0.040 | 4 | 54285923 | missense variant | G/A | snv | 1 | |||
| rs1057519814 | 1.000 | 0.040 | 4 | 54285934 | missense variant | C/T | snv | 1 | |||
| rs1057519815 | 1.000 | 0.040 | 3 | 12599696 | missense variant | C/G | snv | 1 | |||
| rs1060502550 | 1.000 | 0.040 | 4 | 54727488 | missense variant | A/G | snv | 1 | |||
| rs1063045 | 1.000 | 0.040 | 8 | 89982791 | synonymous variant | C/T | snv | 0.35 | 0.33 | 1 | |
| rs10852628 | 1.000 | 0.040 | 16 | 90013519 | intron variant | C/A;T | snv | 1 | |||
| rs11076650 | 1.000 | 0.040 | 16 | 90001533 | non coding transcript exon variant | G/A | snv | 0.49 | 1 | ||
| rs11263498 | 1.000 | 0.040 | 11 | 69567999 | TF binding site variant | T/C | snv | 0.51 | 1 | ||
| rs11551405 | 1.000 | 0.040 | 3 | 53284850 | 3 prime UTR variant | C/A | snv | 0.16 | 1 | ||
| rs11552823 | 1.000 | 0.040 | 9 | 21971117 | missense variant | G/A;C | snv | 4.3E-06 | 1 | ||
| rs1156242341 | 1.000 | 0.040 | 2 | 222202072 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs11568953 | 1.000 | 0.040 | 4 | 109963240 | synonymous variant | A/G | snv | 9.7E-03 | 1.0E-02 | 1 | |
| rs11648898 | 1.000 | 0.040 | 16 | 89979578 | non coding transcript exon variant | A/G | snv | 0.17 | 1 | ||
| rs1176796243 | 1.000 | 0.040 | 3 | 69941240 | missense variant | A/G | snv | 1 | |||
| rs1194330242 | 1.000 | 0.040 | 16 | 4681743 | missense variant | A/G | snv | 1.4E-05 | 1 | ||
| rs121909234 | 1.000 | 0.040 | 10 | 87957867 | missense variant | G/A | snv | 1 | |||
| rs121913225 | 1.000 | 0.040 | 7 | 140753351 | missense variant | A/G | snv | 1 | |||
| rs121913226 | 1.000 | 0.040 | 7 | 140753332 | inframe deletion | TTT/- | del | 1 | |||
| rs121913248 | 1.000 | 0.040 | 1 | 114716109 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs121913363 | 1.000 | 0.040 | 7 | 140753361 | missense variant | T/C | snv | 1 |