| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7683315 | 1.000 | 0.080 | 4 | 87851943 | intergenic variant | T/A;C | snv | 2 | |||
| rs780508132 | 0.925 | 0.080 | X | 32386352 | missense variant | T/A | snv | 5.5E-06 | 1.9E-05 | 2 | |
| rs784288 | 1.000 | 0.080 | 3 | 169253443 | intron variant | A/G;T | snv | 2 | |||
| rs10203122 | 1.000 | 0.080 | 2 | 199831723 | intron variant | T/C | snv | 0.16 | 1 | ||
| rs104895278 | 1.000 | 0.080 | 12 | 6333469 | missense variant | C/T | snv | 2.3E-04 | 3.5E-05 | 1 | |
| rs10832915 | 1.000 | 0.080 | 11 | 18269516 | intron variant | T/C;G | snv | 1 | |||
| rs1181712311 | 1.000 | 0.080 | 19 | 35371499 | missense variant | C/T | snv | 1.5E-05 | 1 | ||
| rs11872467 | 1.000 | 0.080 | 18 | 9848005 | intron variant | G/A | snv | 3.4E-02 | 1 | ||
| rs12151790 | 1.000 | 0.080 | 2 | 234302083 | regulatory region variant | G/A | snv | 0.13 | 1 | ||
| rs1230399 | 1.000 | 0.080 | 17 | 43768035 | 3 prime UTR variant | C/T | snv | 0.66 | 1 | ||
| rs1255801434 | 1.000 | 0.080 | 5 | 102438650 | missense variant | T/C | snv | 4.3E-06 | 1 | ||
| rs1256044 | 1.000 | 0.080 | 14 | 64267309 | intron variant | G/A | snv | 0.66 | 1 | ||
| rs12775980 | 1.000 | 0.080 | 10 | 29570927 | intron variant | C/A;T | snv | 1 | |||
| rs12808199 | 1.000 | 0.080 | 11 | 39306409 | intergenic variant | G/A | snv | 0.47 | 1 | ||
| rs140121121 | 1.000 | 0.080 | X | 115629281 | synonymous variant | T/A | snv | 1.5E-02 | 1.3E-02 | 1 | |
| rs1440203097 | 1.000 | 0.080 | 2 | 96116013 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs145438594 | 1.000 | 0.080 | 12 | 47879073 | missense variant | C/G;T | snv | 1 | |||
| rs1471400 | 1.000 | 0.080 | 4 | 87853095 | regulatory region variant | G/A | snv | 0.38 | 1 | ||
| rs147522958 | 1.000 | 0.080 | 11 | 64564318 | missense variant | G/A | snv | 4.9E-04 | 3.1E-04 | 1 | |
| rs16965654 | 1.000 | 0.080 | 17 | 27280666 | non coding transcript exon variant | G/A | snv | 1.6E-02 | 1 | ||
| rs17184557 | 1.000 | 0.080 | 18 | 69475621 | intron variant | T/A | snv | 0.19 | 1 | ||
| rs17289263 | 1.000 | 0.080 | 9 | 14720363 | synonymous variant | T/C | snv | 9.2E-02 | 9.6E-02 | 1 | |
| rs1751492 | 1.000 | 0.080 | 1 | 65526942 | intron variant | C/A;T | snv | 1 | |||
| rs17651 | 1.000 | 0.080 | 1 | 1014228 | missense variant | G/A;C | snv | 1 | |||
| rs1784235 | 1.000 | 0.080 | 11 | 68418032 | intron variant | C/T | snv | 0.69 | 1 |