| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4869313 | 0.724 | 0.240 | 5 | 96888176 | intron variant | T/A;G | snv | 14 | |||
| rs2910686 | 0.827 | 0.120 | 5 | 96916885 | intron variant | T/C | snv | 0.42 | 5 | ||
| rs1363907 | 1.000 | 0.040 | 5 | 96917099 | intron variant | G/A | snv | 0.38 | 2 | ||
| rs4869314 | 5 | 96893521 | intron variant | G/T | snv | 0.52 | 1 | ||||
| rs2549794 | 1.000 | 0.040 | 5 | 96908845 | intron variant | C/T | snv | 0.62 | 1 | ||
| rs17408150 | 5 | 96903554 | missense variant | T/A | snv | 4.0E-02 | 3.8E-02 | 1 | |||
| rs2927608 | 5 | 96916728 | intron variant | G/A | snv | 0.42 | 1 | ||||
| rs11455840 | 5 | 96910265 | non coding transcript exon variant | AA/-;A;AAA;AAAA;AAAAA;AAAAAAAAAAA | delins | 1 | |||||
| rs34261036 | 5 | 96895352 | missense variant | T/C;G | snv | 4.0E-06; 4.1E-03 | 1 |