| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34424986 | 0.752 | 0.200 | 6 | 161785820 | missense variant | G/A;T | snv | 1.9E-03; 8.0E-06 | 10 | ||
| rs767543900 | 0.790 | 0.120 | 17 | 45971879 | missense variant | A/C;G | snv | 4.0E-06 | 10 | ||
| rs1137070 | 0.763 | 0.160 | X | 43744144 | synonymous variant | T/C | snv | 0.62 | 9 | ||
| rs1169089134 | 0.790 | 0.320 | 11 | 49206785 | missense variant | C/G;T | snv | 9 | |||
| rs188286943 | 0.776 | 0.160 | 16 | 46662452 | missense variant | C/T | snv | 9 | |||
| rs33949390 | 0.776 | 0.160 | 12 | 40320043 | missense variant | G/A;C;T | snv | 1.6E-04; 1.9E-03; 8.0E-06 | 9 | ||
| rs35870237 | 0.763 | 0.120 | 12 | 40340404 | missense variant | T/C | snv | 9 | |||
| rs3849942 | 0.776 | 0.200 | 9 | 27543283 | non coding transcript exon variant | T/A;C | snv | 9 | |||
| rs431905511 | 0.827 | 0.080 | 4 | 89828154 | missense variant | C/T | snv | 9 | |||
| rs6267 | 0.827 | 0.200 | 22 | 19962740 | missense variant | G/A;T | snv | 4.8E-05; 1.4E-02 | 9 | ||
| rs17587 | 0.807 | 0.280 | 6 | 32857313 | missense variant | G/A;T | snv | 0.24; 4.1E-06; 4.1E-06 | 8 | ||
| rs1800955 | 0.827 | 0.160 | 11 | 636784 | upstream gene variant | T/C;G | snv | 8 | |||
| rs628031 | 0.807 | 0.280 | 6 | 160139813 | missense variant | A/C;G | snv | 5.3E-05; 0.63 | 8 | ||
| rs6656401 | 0.776 | 0.200 | 1 | 207518704 | intron variant | A/G;T | snv | 8 | |||
| rs774005786 | 0.790 | 0.080 | 1 | 7970951 | missense variant | G/A;T | snv | 3.9E-04; 2.0E-05 | 8 | ||
| rs104894104 | 0.790 | 0.160 | 9 | 21971019 | missense variant | G/A;T | snv | 7 | |||
| rs11931074 | 0.851 | 0.080 | 4 | 89718364 | intron variant | G/A;C;T | snv | 7 | |||
| rs1799836 | 0.790 | 0.160 | X | 43768752 | intron variant | T/A;C | snv | 0.43 | 7 | ||
| rs2287161 | 0.827 | 0.080 | 12 | 106987362 | upstream gene variant | C/G;T | snv | 7 | |||
| rs2295633 | 0.827 | 0.120 | 1 | 46408711 | intron variant | A/G;T | snv | 7 | |||
| rs28938172 | 0.790 | 0.080 | 1 | 7984981 | missense variant | T/C | snv | 7 | |||
| rs35801418 | 0.827 | 0.120 | 12 | 40321114 | missense variant | A/G | snv | 7 | |||
| rs62643364 | 0.851 | 0.160 | 20 | 4699466 | synonymous variant | A/G;T | snv | 4.0E-06; 1.4E-04 | 7 | ||
| rs7133914 | 0.790 | 0.120 | 12 | 40309109 | missense variant | G/A;T | snv | 8.5E-02; 1.6E-05 | 7 | ||
| rs7308720 | 0.790 | 0.120 | 12 | 40263898 | missense variant | C/A;G | snv | 4.0E-06; 8.7E-02 | 7 |