Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10049390 | 0.776 | 0.080 | 3 | 133982275 | intron variant | G/A | snv | 0.67 | 10 | ||
rs1011970 | 0.677 | 0.320 | 9 | 22062135 | intron variant | G/T | snv | 0.23 | 22 | ||
rs10152518 | 0.790 | 0.080 | 15 | 67884824 | intergenic variant | G/A;T | snv | 9 | |||
rs1028166 | 0.790 | 0.080 | 4 | 181892145 | intron variant | G/A | snv | 0.74 | 9 | ||
rs1035209 | 0.790 | 0.080 | 10 | 99585609 | intergenic variant | C/T | snv | 0.15 | 9 | ||
rs10411210 | 0.742 | 0.160 | 19 | 33041394 | intron variant | C/T | snv | 0.22 | 13 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs10457678 | 0.790 | 0.080 | 6 | 138801103 | intron variant | A/G | snv | 0.19 | 10 | ||
rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 71 | ||
rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 73 | |||
rs10505477 | 0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 | 31 | ||
rs10506868 | 0.716 | 0.160 | 10 | 112559621 | intron variant | C/T | snv | 3.1E-02 | 16 | ||
rs10511330 | 0.776 | 0.080 | 3 | 114402172 | intron variant | T/C | snv | 0.22 | 10 | ||
rs1057519738 | 0.790 | 0.160 | 17 | 39725079 | missense variant | G/A | snv | 4.0E-06 | 10 | ||
rs1057519739 | 1.000 | 0.080 | 18 | 51065518 | missense variant | G/A;C | snv | 2 | |||
rs1057519890 | 0.807 | 0.200 | 17 | 39723966 | missense variant | T/A | snv | 8 | |||
rs1057519895 | 0.724 | 0.240 | 4 | 152328232 | missense variant | C/A;G;T | snv | 17 | |||
rs1057519943 | 0.790 | 0.160 | 12 | 132676598 | missense variant | G/C;T | snv | 10 | |||
rs1057941 | 0.701 | 0.280 | 1 | 155216951 | non coding transcript exon variant | G/A;T | snv | 0.46 | 18 | ||
rs10774214 | 0.790 | 0.080 | 12 | 4259186 | intron variant | T/C | snv | 0.54 | 9 | ||
rs1078643 | 0.776 | 0.080 | 17 | 10803924 | missense variant | G/A;C | snv | 10 | |||
rs10795668 | 0.724 | 0.160 | 10 | 8659256 | upstream gene variant | G/A | snv | 0.24 | 17 | ||
rs10808555 | 0.925 | 0.080 | 8 | 127397266 | intron variant | G/A | snv | 0.65 | 6 | ||
rs10821907 | 0.776 | 0.080 | 10 | 50888694 | upstream gene variant | C/T | snv | 0.20 | 12 | ||
rs10849432 | 0.790 | 0.080 | 12 | 6276561 | intergenic variant | C/T | snv | 0.84 | 9 |