Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057518083 | 0.851 | 0.120 | 14 | 101986552 | missense variant | C/T | snv | 21 | |||
rs362569 | 1.000 | 0.040 | 20 | 10266085 | intron variant | T/C | snv | 0.38 | 1 | ||
rs227283 | 0.925 | 0.120 | 4 | 102686096 | intron variant | C/G;T | snv | 2 | |||
rs6108461 | 1.000 | 0.040 | 20 | 10286622 | intron variant | A/G | snv | 0.57 | 1 | ||
rs362549 | 1.000 | 0.040 | 20 | 10289242 | intron variant | A/G | snv | 0.56 | 1 | ||
rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 9 | ||
rs362990 | 1.000 | 0.040 | 20 | 10295573 | intron variant | A/T | snv | 0.23 | 1 | ||
rs362998 | 1.000 | 0.040 | 20 | 10296973 | synonymous variant | C/T | snv | 0.11 | 0.11 | 1 | |
rs7914558 | 0.851 | 0.040 | 10 | 103016151 | intron variant | G/A | snv | 0.40 | 5 | ||
rs3746544 | 0.790 | 0.120 | 20 | 10306436 | 3 prime UTR variant | G/T | snv | 0.68 | 10 | ||
rs1051312 | 0.827 | 0.120 | 20 | 10306440 | 3 prime UTR variant | T/C | snv | 0.20 | 5 | ||
rs8636 | 1.000 | 0.040 | 20 | 10307094 | 3 prime UTR variant | T/A;C | snv | 1 | |||
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 13 | ||
rs736707 | 0.851 | 0.040 | 7 | 103489956 | intron variant | A/G | snv | 0.30 | 6 | ||
rs7341475 | 0.851 | 0.240 | 7 | 103764368 | intron variant | G/A | snv | 0.17 | 6 | ||
rs1592757 | 1.000 | 0.040 | 5 | 104554297 | intron variant | G/C | snv | 0.29 | 1 | ||
rs325485 | 0.925 | 0.120 | 5 | 104659667 | intron variant | A/G | snv | 0.65 | 2 | ||
rs11591402 | 1.000 | 0.040 | 10 | 104987596 | intron variant | T/A;G | snv | 1 | |||
rs9297357 | 0.851 | 0.040 | 8 | 105130105 | intron variant | C/G;T | snv | 5 | |||
rs11074889 | 1.000 | 0.040 | 16 | 10539308 | intron variant | A/G;T | snv | 1 | |||
rs6539247 | 1.000 | 0.040 | 12 | 106066124 | 3 prime UTR variant | T/C;G | snv | 1 | |||
rs2230460 | 0.925 | 0.040 | 7 | 106884244 | synonymous variant | C/T | snv | 0.12 | 8.5E-02 | 2 | |
rs12536620 | 1.000 | 0.040 | 7 | 106904783 | intron variant | A/G | snv | 0.42 | 1 | ||
rs12667819 | 1.000 | 0.040 | 7 | 106906212 | 3 prime UTR variant | G/A | snv | 0.41 | 1 | ||
rs12871532 | 0.851 | 0.040 | 13 | 108016199 | intergenic variant | T/C | snv | 0.46 | 5 |