| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1437969513 | 1.000 | 0.040 | 6 | 1611203 | missense variant | C/T | snv | 1.1E-05 | 1 | ||
| rs77888940 | 1.000 | 0.040 | 6 | 1610017 | 5 prime UTR variant | C/A;G;T | snv | 1 | |||
| rs886041355 | 1.000 | 0.040 | 6 | 1610901 | stop gained | G/A | snv | 1 | |||
| rs555091 | 1.000 | 0.040 | 11 | 31511412 | 3 prime UTR variant | T/C | snv | 5.6E-03 | 1 | ||
| rs945686 | 1.000 | 0.040 | 9 | 126615747 | intron variant | G/C;T | snv | 1 | |||
| rs187112398 | 1.000 | 0.040 | 15 | 75756813 | intron variant | C/T | snv | 7.6E-04 | 1 | ||
| rs1035650739 | 1.000 | 0.040 | 19 | 50362252 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs2437812 | 1.000 | 0.040 | 9 | 104930920 | upstream gene variant | A/C;T | snv | 1 | |||
| rs11710139 | 1.000 | 0.040 | 3 | 150341555 | non coding transcript exon variant | G/A | snv | 0.21 | 1 | ||
| rs2304719 | 1.000 | 0.040 | 15 | 73943159 | intron variant | C/T | snv | 0.30 | 1 | ||
| rs4243042 | 1.000 | 0.040 | 15 | 73949283 | intron variant | A/T | snv | 0.37 | 1 | ||
| rs893817 | 1.000 | 0.040 | 15 | 73936724 | intron variant | G/A | snv | 0.67 | 1 | ||
| rs1210326005 | 1.000 | 0.040 | 15 | 73927510 | missense variant | C/G;T | snv | 1.2E-05 | 1 | ||
| rs73174345 | 1.000 | 0.040 | 3 | 169535095 | intron variant | T/G | snv | 7.9E-02 | 1 | ||
| rs750585311 | 1.000 | 0.040 | 1 | 171652499 | missense variant | C/T | snv | 1 | |||
| rs879255525 | 1.000 | 0.040 | 1 | 171636617 | stop gained | T/A | snv | 4.0E-06 | 1 | ||
| rs113432289 | 1.000 | 0.040 | 7 | 22253498 | intron variant | A/C | snv | 3.3E-03 | 1 | ||
| rs192917960 | 1.000 | 0.040 | 16 | 5869654 | intron variant | C/A;T | snv | 1 | |||
| rs7114303 | 1.000 | 0.040 | 11 | 10074140 | intron variant | G/C | snv | 0.28 | 1 | ||
| rs754992859 | 1.000 | 0.040 | X | 30855520 | missense variant | C/T | snv | 5.7E-06 | 1 | ||
| rs12699251 | 1.000 | 0.040 | 7 | 11639486 | intron variant | A/G | snv | 0.33 | 1 | ||
| rs869833 | 1.000 | 0.040 | 2 | 102766672 | intron variant | T/C | snv | 0.49 | 1 | ||
| rs553774660 | 1.000 | 0.040 | 11 | 89178097 | missense variant | G/T | snv | 1 | |||
| rs1438561194 | 1.000 | 0.040 | 5 | 111092304 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs35703638 | 1.000 | 0.040 | 5 | 111106140 | missense variant | G/A | snv | 8.3E-03 | 4.1E-03 | 1 |