| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13286166 | 1.000 | 0.080 | 9 | 741307 | intron variant | G/A;T | snv | 1 | |||
| rs4742225 | 1.000 | 0.080 | 9 | 677938 | intron variant | G/T | snv | 0.50 | 1 | ||
| rs2273505 | 1.000 | 0.080 | 20 | 63359526 | non coding transcript exon variant | C/T | snv | 4.0E-06; 9.2E-02 | 9.5E-02 | 1 | |
| rs4845652 | 1.000 | 0.080 | 1 | 154565729 | non coding transcript exon variant | C/A;T | snv | 1 | |||
| rs10865246 | 1.000 | 0.080 | 2 | 50443116 | intron variant | C/A;T | snv | 1 | |||
| rs1122530 | 1.000 | 0.080 | 9 | 84849437 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs1187272 | 1.000 | 0.080 | 9 | 84789171 | intron variant | G/A;C | snv | 1 | |||
| rs1659400 | 1.000 | 0.080 | 9 | 84711079 | intron variant | A/G | snv | 0.60 | 1 | ||
| rs4075274 | 1.000 | 0.080 | 9 | 84981647 | intron variant | T/C | snv | 0.50 | 1 | ||
| rs729560 | 1.000 | 0.080 | 9 | 85019390 | intron variant | G/A | snv | 0.74 | 1 | ||
| rs736744 | 1.000 | 0.080 | 9 | 84899492 | intron variant | C/T | snv | 0.45 | 1 | ||
| rs920776 | 1.000 | 0.080 | 9 | 84923421 | intron variant | G/A | snv | 0.18 | 1 | ||
| rs993315 | 1.000 | 0.080 | 9 | 84672806 | intron variant | T/C | snv | 0.50 | 1 | ||
| rs557748 | 1.000 | 0.080 | 6 | 154043167 | intron variant | G/A | snv | 0.19 | 1 | ||
| rs774507706 | 1.000 | 0.080 | 6 | 154091093 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs17710 | 1.000 | 0.080 | 17 | 7240675 | 3 prime UTR variant | A/T | snv | 0.10 | 1 | ||
| rs2878298 | 1.000 | 0.080 | 3 | 49368647 | intron variant | T/C | snv | 0.43 | 1 | ||
| rs12519 | 1.000 | 0.080 | 9 | 89013167 | 3 prime UTR variant | T/A;C | snv | 1 | |||
| rs1331188 | 1.000 | 0.080 | 9 | 89110472 | intron variant | G/T | snv | 0.23 | 1 | ||
| rs1411836 | 1.000 | 0.080 | 9 | 89160966 | intron variant | C/G;T | snv | 0.12 | 1 | ||
| rs1547696 | 1.000 | 0.080 | 9 | 89079205 | intron variant | T/C | snv | 0.60 | 1 | ||
| rs1556384 | 1.000 | 0.080 | 9 | 89149212 | intron variant | T/C | snv | 0.93 | 1 | ||
| rs2297313 | 1.000 | 0.080 | 9 | 89054447 | intron variant | A/G | snv | 0.41 | 1 | ||
| rs3750399 | 1.000 | 0.080 | 9 | 89042048 | synonymous variant | T/A;C | snv | 0.71 | 1 | ||
| rs3818668 | 1.000 | 0.080 | 9 | 89065616 | intron variant | C/G | snv | 0.76 | 0.64 | 1 |