| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs75389940 | 0.882 | 0.120 | 7 | 117627753 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
| rs1078761 | 1.000 | 0.120 | 20 | 33288875 | missense variant | A/C;G | snv | 4.1E-06; 0.30 | 2 | ||
| rs1143639 | 1.000 | 0.120 | 2 | 112831216 | non coding transcript exon variant | C/T | snv | 0.20 | 2 | ||
| rs146521846 | 0.925 | 0.120 | 7 | 117611794 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 2 | ||
| rs150157202 | 0.925 | 0.120 | 7 | 117592427 | missense variant | G/A;T | snv | 1.8E-03 | 1.7E-03 | 2 | |
| rs1800080 | 0.925 | 0.120 | 7 | 117534330 | missense variant | A/G | snv | 2 | |||
| rs2077079 | 0.925 | 0.120 | 2 | 85668215 | missense variant | T/G | snv | 0.41 | 0.39 | 2 | |
| rs2734705 | 0.925 | 0.120 | 1 | 86486641 | missense variant | A/G | snv | 0.86 | 0.87 | 2 | |
| rs397508185 | 0.925 | 0.120 | 7 | 117548684 | missense variant | A/G | snv | 2.8E-05 | 2.8E-05 | 2 | |
| rs1057516619 | 1.000 | 0.120 | 7 | 117536669 | stop gained | A/T | snv | 1 | |||
| rs1059057 | 1.000 | 0.120 | 10 | 79613765 | synonymous variant | A/G | snv | 9.9E-02 | 6.4E-02 | 1 | |
| rs1136451 | 1.000 | 0.120 | 10 | 79612325 | synonymous variant | A/G | snv | 0.21 | 0.17 | 1 | |
| rs121909010 | 1.000 | 0.120 | 7 | 117652915 | stop gained | G/A | snv | 1 | |||
| rs121909034 | 1.000 | 0.120 | 7 | 117603609 | stop gained | C/A;T | snv | 1.1E-03 | 1 | ||
| rs1396707015 | 1.000 | 0.120 | 7 | 117535273 | stop gained | G/A | snv | 1 | |||
| rs139729994 | 0.925 | 0.120 | 7 | 117614713 | missense variant | G/A;T | snv | 4.0E-06; 1.3E-04 | 1 | ||
| rs144745159 | 1.000 | 0.120 | 7 | 117587770 | missense variant | T/C | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs149353983 | 1.000 | 0.120 | 7 | 117504291 | missense variant | G/A;T | snv | 5.6E-05; 3.2E-05 | 1 | ||
| rs1626154 | 1.000 | 0.120 | 11 | 73235159 | missense variant | C/A;G;T | snv | 4.1E-06; 1.0E-04; 0.15 | 1 | ||
| rs17140229 | 1.000 | 0.120 | 7 | 117590229 | intron variant | T/C | snv | 9.9E-02 | 1 | ||
| rs193922525 | 1.000 | 0.120 | 7 | 117664770 | missense variant | G/A | snv | 1 | |||
| rs200901072 | 1.000 | 0.120 | 7 | 117603610 | synonymous variant | G/A;C;T | snv | 4.8E-05; 8.0E-06; 4.0E-06 | 1 | ||
| rs2511241 | 1.000 | 0.120 | 11 | 73234296 | missense variant | C/G;T | snv | 4.0E-06; 0.93 | 1 | ||
| rs3024798 | 1.000 | 0.120 | 2 | 85667185 | splice region variant | G/A;T | snv | 0.36 | 1 | ||
| rs3741156 | 1.000 | 0.120 | 11 | 73235095 | missense variant | G/A;C | snv | 0.29 | 0.20 | 1 |