| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12136973 | 1.000 | 0.080 | 1 | 175171183 | intron variant | T/C | snv | 0.22 | 3 | ||
| rs113247976 | 1.000 | 0.080 | 12 | 57581917 | missense variant | C/G;T | snv | 4.0E-06; 1.1E-02 | 2 | ||
| rs1360444859 | 1.000 | 0.080 | 16 | 1791721 | missense variant | T/C | snv | 1.2E-05 | 2 | ||
| rs149215094 | 1.000 | 0.080 | 20 | 58444203 | missense variant | G/A | snv | 5.6E-05 | 5.6E-05 | 2 | |
| rs58599399 | 1.000 | 0.080 | 12 | 49295621 | missense variant | G/A;T | snv | 3.2E-03 | 2 | ||
| rs695871 | 1.000 | 0.080 | 12 | 111599196 | missense variant | G/C | snv | 0.77 | 0.61 | 2 | |
| rs749191312 | 1.000 | 0.080 | 20 | 18497075 | synonymous variant | C/T | snv | 4.0E-06 | 2 | ||
| rs760555162 | 1.000 | 0.080 | 12 | 6537178 | synonymous variant | G/A | snv | 4.0E-06 | 2 | ||
| rs771884087 | 1.000 | 0.080 | 20 | 45253726 | synonymous variant | T/C | snv | 2 | |||
| rs775018856 | 1.000 | 0.080 | 17 | 7283304 | synonymous variant | G/A | snv | 2.8E-05 | 1.4E-05 | 2 | |
| rs1008459 | 1.000 | 0.080 | 1 | 175182047 | intron variant | T/C | snv | 0.25 | 1 | ||
| rs10122902 | 1.000 | 0.080 | 9 | 27556782 | synonymous variant | G/A | snv | 0.24 | 0.21 | 1 | |
| rs10143310 | 1.000 | 0.080 | 14 | 92074037 | intron variant | G/A;C | snv | 1 | |||
| rs1032968973 | 1.000 | 0.080 | 1 | 156842164 | synonymous variant | A/G | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs10438933 | 1.000 | 0.080 | 18 | 31693166 | intergenic variant | A/G | snv | 0.14 | 1 | ||
| rs10463311 | 1.000 | 0.080 | 5 | 151031274 | intron variant | C/T | snv | 0.66 | 1 | ||
| rs10511816 | 1.000 | 0.080 | 9 | 27468463 | intron variant | C/A | snv | 0.30 | 1 | ||
| rs1053983726 | 1.000 | 0.080 | 1 | 28150741 | missense variant | C/G | snv | 1 | |||
| rs1054281443 | 1.000 | 0.080 | 11 | 3735207 | missense variant | G/A | snv | 4.1E-06 | 1 | ||
| rs10757665 | 1.000 | 0.080 | 9 | 27557921 | intron variant | T/C | snv | 0.20 | 1 | ||
| rs10812605 | 1.000 | 0.080 | 9 | 27510362 | intron variant | C/T | snv | 0.58 | 1 | ||
| rs10812611 | 1.000 | 0.080 | 9 | 27542263 | non coding transcript exon variant | C/T | snv | 0.42 | 1 | ||
| rs10967952 | 1.000 | 0.080 | 9 | 27474216 | intron variant | T/C | snv | 0.17 | 1 | ||
| rs10967958 | 1.000 | 0.080 | 9 | 27481907 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs10967959 | 1.000 | 0.080 | 9 | 27482969 | intron variant | C/G;T | snv | 1 |