| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1236515917 | 1.000 | 0.080 | 9 | 21367798 | missense variant | C/G | snv | 4.4E-06 | 1 | ||
| rs1303234079 | 1.000 | 0.080 | 7 | 143267656 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs13401937 | 1.000 | 0.080 | 2 | 55025078 | splice region variant | T/G | snv | 0.11 | 0.14 | 1 | |
| rs1484994 | 1.000 | 0.080 | 20 | 31718172 | intron variant | A/G | snv | 0.38 | 1 | ||
| rs1754257 | 1.000 | 0.080 | 10 | 25385685 | intron variant | G/A | snv | 0.71 | 1 | ||
| rs179012 | 1.000 | 0.080 | X | 12883443 | intron variant | G/A | snv | 0.42 | 1 | ||
| rs179016 | 1.000 | 0.080 | X | 12876323 | intron variant | G/A;C;T | snv | 1 | |||
| rs1800803 | 1.000 | 0.080 | 4 | 99574424 | intron variant | A/T | snv | 0.43 | 1 | ||
| rs1979860 | 1.000 | 0.080 | 5 | 174586529 | regulatory region variant | C/T | snv | 1.8E-02 | 1 | ||
| rs1997060 | 1.000 | 0.080 | 3 | 174035108 | intron variant | A/G | snv | 0.18 | 1 | ||
| rs200664537 | 1.000 | 0.080 | 8 | 11847084 | missense variant | G/A;C | snv | 4.0E-06; 1.2E-04 | 1 | ||
| rs201065145 | 1.000 | 0.080 | 8 | 144505096 | missense variant | G/A | snv | 1.4E-04 | 3.5E-05 | 1 | |
| rs2233437 | 1.000 | 0.080 | 6 | 44260425 | intron variant | G/A | snv | 0.43 | 0.35 | 1 | |
| rs2278034 | 1.000 | 0.080 | 3 | 195870036 | 3 prime UTR variant | T/C;G | snv | 0.44; 2.7E-05 | 1 | ||
| rs2284191 | 1.000 | 0.080 | 6 | 33008877 | intron variant | G/A | snv | 7.5E-02 | 1 | ||
| rs2492965 | 1.000 | 0.080 | 6 | 72445473 | intergenic variant | T/C | snv | 0.90 | 1 | ||
| rs2569540 | 1.000 | 0.080 | 19 | 11127563 | non coding transcript exon variant | C/G | snv | 0.68 | 1 | ||
| rs2647006 | 1.000 | 0.080 | 6 | 32692805 | intergenic variant | A/C;G | snv | 1 | |||
| rs2647051 | 1.000 | 0.080 | 6 | 32703120 | downstream gene variant | T/C | snv | 0.64 | 1 | ||
| rs28362857 | 1.000 | 0.080 | 6 | 44265479 | missense variant | G/A;C | snv | 8.3E-06; 3.1E-02 | 1 | ||
| rs28372683 | 1.000 | 0.080 | 19 | 45038140 | 3 prime UTR variant | G/A;T | snv | 1 | |||
| rs3128925 | 1.000 | 0.080 | 6 | 33103823 | non coding transcript exon variant | C/A;T | snv | 1 | |||
| rs3212172 | 1.000 | 0.080 | 20 | 44399750 | intron variant | A/C;G | snv | 1 | |||
| rs35384524 | 1.000 | 0.080 | 21 | 21017373 | intron variant | C/G;T | snv | 1 | |||
| rs3733096 | 1.000 | 0.080 | 3 | 46202483 | 3 prime UTR variant | C/G | snv | 1.4E-03 | 1 |