Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 43 | ||
rs1800440 | 0.653 | 0.440 | 2 | 38070996 | missense variant | T/C;G | snv | 0.15; 4.0E-06 | 29 | ||
rs5743618 | 0.677 | 0.360 | 4 | 38797027 | missense variant | C/A | snv | 0.53 | 0.51 | 25 | |
rs174535 | 0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 | 19 | |
rs1689510 | 0.724 | 0.240 | 12 | 56002984 | non coding transcript exon variant | G/C | snv | 0.25 | 16 | ||
rs4129267 | 0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv | 13 | |||
rs3939286 | 0.776 | 0.360 | 9 | 6210099 | regulatory region variant | T/A;C | snv | 12 | |||
rs1837253 | 0.790 | 0.240 | 5 | 111066174 | upstream gene variant | T/C | snv | 0.72 | 10 | ||
rs4845604 | 0.776 | 0.200 | 1 | 151829204 | intron variant | G/A;C;T | snv | 10 | |||
rs112401631 | 0.882 | 0.120 | 17 | 40608272 | TF binding site variant | T/A | snv | 1.1E-02 | 8 | ||
rs34290285 | 0.851 | 0.120 | 2 | 241759225 | intron variant | G/A | snv | 0.27 | 8 | ||
rs17454584 | 0.851 | 0.080 | 4 | 122432277 | downstream gene variant | A/G | snv | 0.17 | 6 | ||
rs2497318 | 0.827 | 0.120 | 10 | 92672243 | upstream gene variant | C/A;T | snv | 6 | |||
rs479844 | 0.851 | 0.160 | 11 | 65784486 | upstream gene variant | A/G | snv | 0.44 | 6 | ||
rs16903574 | 0.882 | 0.120 | 5 | 14610200 | missense variant | C/A;G | snv | 4.0E-06; 5.6E-02 | 6 | ||
rs72743461 | 0.827 | 0.160 | 15 | 67149412 | intron variant | C/A;T | snv | 6 | |||
rs117710327 | 0.882 | 0.080 | 19 | 33235672 | TF binding site variant | C/A | snv | 5.0E-02 | 5 | ||
rs12365699 | 0.882 | 0.120 | 11 | 118872577 | regulatory region variant | G/A | snv | 0.12 | 5 | ||
rs7936312 | 0.882 | 0.080 | 11 | 76582682 | intergenic variant | G/T | snv | 0.44 | 5 | ||
rs3785356 | 0.925 | 0.080 | 16 | 27337847 | intron variant | C/T | snv | 0.25 | 5 | ||
rs34712979 | 1.000 | 0.040 | 4 | 105897896 | splice region variant | G/A;T | snv | 0.17 | 5 | ||
rs9979383 | 0.925 | 0.200 | 21 | 35343463 | intron variant | C/G;T | snv | 5 | |||
rs903361 | 0.882 | 0.160 | 1 | 203122146 | intron variant | G/A;C | snv | 4 | |||
rs3749833 | 0.925 | 0.080 | 5 | 132463934 | non coding transcript exon variant | T/C | snv | 0.23 | 4 | ||
rs12123821 | 0.925 | 0.080 | 1 | 152206676 | intron variant | C/T | snv | 2.9E-02 | 4 |