| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1036819 | 0.925 | 0.120 | 8 | 134599702 | non coding transcript exon variant | A/C | snv | 0.11 | 2 | ||
| rs1038025 | 1.000 | 0.080 | 19 | 44901715 | 3 prime UTR variant | T/C;G | snv | 1 | |||
| rs1038026 | 1.000 | 0.080 | 19 | 44901805 | 3 prime UTR variant | A/G;T | snv | 4 | |||
| rs1038162399 | 0.925 | 0.080 | 21 | 25911954 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
| rs10399931 | 0.807 | 0.320 | 1 | 203186952 | upstream gene variant | T/A;C | snv | 6 | |||
| rs10401176 | 1.000 | 0.080 | 19 | 44750234 | intron variant | C/G;T | snv | 0.17 | 2 | ||
| rs10402271 | 1.000 | 0.080 | 19 | 44825957 | downstream gene variant | T/G | snv | 0.28 | 7 | ||
| rs10405693 | 1.000 | 0.080 | 19 | 44823407 | downstream gene variant | C/T | snv | 0.28 | 1 | ||
| rs10407439 | 1.000 | 0.080 | 19 | 44838691 | intergenic variant | A/G | snv | 0.69 | 1 | ||
| rs10408847 | 1.000 | 0.080 | 19 | 45131424 | intron variant | G/C | snv | 0.26 | 1 | ||
| rs10410544 | 0.827 | 0.120 | 19 | 38894892 | intron variant | T/C | snv | 0.68 | 0.67 | 6 | |
| rs10412413 | 1.000 | 0.080 | 19 | 44824052 | downstream gene variant | C/T | snv | 0.30 | 1 | ||
| rs10415983 | 1.000 | 0.080 | 19 | 45208340 | intron variant | C/T | snv | 0.26 | 1 | ||
| rs10416371 | 1.000 | 0.080 | 19 | 45156878 | intron variant | A/C;T | snv | 1 | |||
| rs1041833271 | 0.925 | 0.080 | 21 | 25975995 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
| rs1042114 | 0.807 | 0.120 | 1 | 28812463 | missense variant | G/C;T | snv | 0.91 | 6 | ||
| rs10421247 | 1.000 | 0.080 | 19 | 45154228 | intron variant | C/T | snv | 0.52 | 1 | ||
| rs10422797 | 1.000 | 0.080 | 19 | 45222848 | intron variant | T/C | snv | 8.9E-02 | 1 | ||
| rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
| rs10426401 | 1.000 | 0.080 | 19 | 44644419 | intron variant | T/G | snv | 0.32 | 2 | ||
| rs10455152 | 1.000 | 0.080 | 6 | 85308630 | intergenic variant | A/C | snv | 0.29 | 1 | ||
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs1047552 | 0.925 | 0.080 | 15 | 63305658 | missense variant | T/A;G | snv | 6.1E-02 | 4.7E-02 | 2 | |
| rs1048218 | 1.000 | 0.080 | 11 | 27658340 | missense variant | C/A | snv | 1 | |||
| rs1048699 | 1.000 | 0.080 | 19 | 45147128 | 3 prime UTR variant | C/T | snv | 9.0E-02 | 2 |