| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28936670 | 0.708 | 0.280 | 5 | 173235011 | missense variant | G/A | snv | 3.4E-03 | 1.1E-02 | 17 | |
| rs1060499548 | 0.724 | 0.440 | 9 | 130872961 | missense variant | G/A | snv | 27 | |||
| rs113624356 | 0.724 | 0.400 | 11 | 66526181 | missense variant | T/G | snv | 1.5E-03 | 2.1E-03 | 22 | |
| rs2277923 | 0.752 | 0.160 | 5 | 173235021 | synonymous variant | T/C | snv | 0.41 | 0.44 | 13 | |
| rs1532268 | 0.776 | 0.280 | 5 | 7878066 | missense variant | C/T | snv | 0.31 | 0.32 | 12 | |
| rs76216585 | 0.807 | 0.160 | 12 | 89492071 | stop gained | C/A;G;T | snv | 8.5E-06; 2.7E-04 | 9 | ||
| rs387906769 | 0.807 | 0.080 | 8 | 11708799 | missense variant | C/T | snv | 7.3E-05 | 4.2E-05 | 7 | |
| rs886037834 | 0.827 | 0.160 | 7 | 47846960 | missense variant | C/G | snv | 7.0E-06 | 6 | ||
| rs870142 | 0.851 | 0.120 | 4 | 4646320 | intron variant | C/G;T | snv | 7 | |||
| rs16835979 | 0.851 | 0.120 | 4 | 4633549 | intron variant | C/A | snv | 0.20 | 6 | ||
| rs6824295 | 0.851 | 0.120 | 4 | 4612553 | intron variant | C/T | snv | 0.20 | 6 | ||
| rs41291957 | 0.882 | 0.200 | 5 | 149428827 | intron variant | G/A | snv | 0.12 | 7 | ||
| rs804280 | 0.882 | 0.120 | 8 | 11755189 | intron variant | C/A;G | snv | 6 | |||
| rs56166237 | 0.882 | 0.120 | 8 | 11708411 | missense variant | G/T | snv | 3.6E-03 | 2.0E-03 | 4 | |
| rs6489957 | 0.925 | 0.120 | 12 | 114355808 | synonymous variant | G/A | snv | 4.4E-03 | 1.7E-02 | 4 | |
| rs121965033 | 0.925 | 0.120 | 4 | 1002333 | missense variant | T/C;G | snv | 4.0E-06 | 3 | ||
| rs137852684 | 0.925 | 0.160 | 5 | 173233189 | missense variant | C/A;T | snv | 9.0E-04 | 3 | ||
| rs368418329 | 0.925 | 0.120 | 8 | 11708019 | 5 prime UTR variant | G/T | snv | 5.9E-03 | 3 | ||
| rs1060499547 | 1.000 | 9 | 130862890 | missense variant | A/G | snv | 4 | ||||
| rs3729753 | 1.000 | 0.040 | 5 | 173232938 | synonymous variant | C/G | snv | 9.9E-03 | 2.2E-03 | 3 | |
| rs387906776 | 1.000 | 0.080 | 5 | 173232775 | missense variant | G/A;C;T | snv | 4.2E-06; 8.4E-06 | 3 | ||
| rs764328696 | 1.000 | 7 | 35248696 | missense variant | C/G;T | snv | 3 | ||||
| rs1017 | 1.000 | 0.040 | 5 | 51394261 | 3 prime UTR variant | A/G;T | snv | 2 | |||
| rs143081213 | 1.000 | 0.040 | 21 | 34615168 | upstream gene variant | G/A | snv | 2.6E-02 | 2 | ||
| rs145641996 | 1.000 | 0.040 | 1 | 11792285 | missense variant | T/C;G | snv | 1.6E-05; 1.6E-04 | 2 |