| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3755266 | 1.000 | 0.080 | 2 | 102426252 | intron variant | G/A | snv | 0.55 | 1 | ||
| rs2310300 | 1.000 | 0.080 | 2 | 102432614 | intron variant | A/G | snv | 0.55 | 1 | ||
| rs917997 | 0.701 | 0.480 | 2 | 102454108 | downstream gene variant | T/A;C | snv | 20 | |||
| rs921877174 | 1.000 | 0.080 | 5 | 102498796 | missense variant | T/C | snv | 1 | |||
| rs866294686 | 0.683 | 0.480 | 10 | 102657073 | stop gained | C/A;T | snv | 43 | |||
| rs227283 | 0.925 | 0.120 | 4 | 102686096 | intron variant | C/G;T | snv | 2 | |||
| rs5491 | 0.827 | 0.160 | 19 | 10274864 | missense variant | A/G;T | snv | 4.0E-06; 2.8E-02 | 6 | ||
| rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
| rs2276109 | 0.701 | 0.440 | 11 | 102875061 | upstream gene variant | T/C | snv | 9.2E-02 | 18 | ||
| rs572527200 | 0.882 | 0.240 | 11 | 102875064 | upstream gene variant | T/C | snv | 4 | |||
| rs696217 | 0.662 | 0.640 | 3 | 10289773 | missense variant | G/T | snv | 8.8E-02 | 7.1E-02 | 32 | |
| rs74380195 | 1.000 | 0.080 | 11 | 103016500 | intergenic variant | A/G | snv | 0.11 | 1 | ||
| rs7921536 | 1.000 | 0.080 | 10 | 103597080 | 3 prime UTR variant | A/G | snv | 3.5E-02 | 1 | ||
| rs12248541 | 1.000 | 0.080 | 10 | 103630585 | intron variant | A/G | snv | 4.2E-02 | 1 | ||
| rs28903081 | 0.851 | 0.200 | 14 | 103698934 | missense variant | C/A;T | snv | 4.5E-06; 4.3E-04 | 5 | ||
| rs538104363 | 1.000 | 0.080 | 8 | 103936637 | missense variant | G/A;T | snv | 1.6E-05; 2.8E-05 | 1 | ||
| rs868696973 | 1.000 | 0.080 | 8 | 103936694 | missense variant | G/A | snv | 4.1E-06 | 1 | ||
| rs1190217503 | 1.000 | 0.080 | 8 | 103942885 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs1307973611 | 1.000 | 0.080 | 8 | 104014523 | missense variant | G/C;T | snv | 2 | |||
| rs1057518581 | 1.000 | 0.080 | 8 | 104014574 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs591118 | 1.000 | 0.080 | 11 | 104095993 | intron variant | A/G | snv | 0.55 | 1 | ||
| rs182290714 | 1.000 | 0.080 | 8 | 104244969 | synonymous variant | C/T | snv | 1.8E-04 | 4.7E-04 | 1 | |
| rs156697 | 0.672 | 0.560 | 10 | 104279427 | missense variant | A/G;T | snv | 0.35 | 25 | ||
| rs325485 | 0.925 | 0.120 | 5 | 104659667 | intron variant | A/G | snv | 0.65 | 2 | ||
| rs396755 | 0.925 | 0.120 | 5 | 104686538 | intron variant | C/G | snv | 0.61 | 2 |