Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
rs6311 | 0.645 | 0.640 | 13 | 46897343 | upstream gene variant | C/T | snv | 0.40 | 41 | ||
rs41423247 | 0.695 | 0.440 | 5 | 143399010 | intron variant | G/C | snv | 0.31 | 23 | ||
rs35761398 | 0.701 | 0.520 | 1 | 23875429 | missense variant | TT/CC | mnv | 19 | |||
rs3798577 | 0.742 | 0.320 | 6 | 152099995 | 3 prime UTR variant | T/C | snv | 0.45 | 16 | ||
rs6198 | 0.724 | 0.480 | 5 | 143278056 | 3 prime UTR variant | T/C | snv | 0.12 | 16 | ||
rs879761216 | 0.732 | 0.480 | 1 | 23875429 | frameshift variant | TT/C;T | delins | 14 | |||
rs13438494 | 1.000 | 0.040 | 7 | 82759398 | intron variant | T/G | snv | 0.61 | 6 | ||
rs1473473 | 0.925 | 0.080 | 12 | 72010598 | intron variant | C/A;T | snv | 0.81 | 4 | ||
rs10858583 | 1.000 | 0.040 | 12 | 87334666 | intergenic variant | C/T | snv | 0.79 | 3 | ||
rs12149074 | 1.000 | 0.040 | 16 | 80071969 | intron variant | C/A;G | snv | 3 | |||
rs13086738 | 1.000 | 0.040 | 3 | 181080939 | intron variant | A/G | snv | 0.21 | 3 | ||
rs17536211 | 1.000 | 0.040 | 4 | 46085716 | intron variant | A/C | snv | 0.14 | 3 | ||
rs1805576 | 1.000 | 0.040 | 3 | 180949777 | intron variant | C/G;T | snv | 0.24 | 3 | ||
rs4148087 | 1.000 | 0.040 | 21 | 42202157 | intron variant | G/A;T | snv | 3 | |||
rs4854912 | 1.000 | 0.040 | 3 | 181063312 | intron variant | C/T | snv | 0.15 | 3 | ||
rs12475512 | 2 | 231433365 | downstream gene variant | G/A | snv | 0.47 | 2 | ||||
rs13077017 | 3 | 58120049 | intron variant | C/T | snv | 0.21 | 2 | ||||
rs1356639869 | 1.000 | 0.040 | 7 | 24289527 | missense variant | C/A | snv | 2 | |||
rs138206701 | 5 | 81110747 | intron variant | A/G | snv | 1.7E-02 | 2 | ||||
rs4869317 | 1.000 | 0.040 | 5 | 96956300 | intron variant | T/A | snv | 0.22 | 2 | ||
rs7322916 | 13 | 25433839 | intron variant | G/A;C | snv | 2 | |||||
rs74566133 | 8 | 133766099 | regulatory region variant | C/T | snv | 2.6E-02 | 2 | ||||
rs7180942 | 15 | 88131345 | intron variant | T/C | snv | 0.56 | 1 | ||||
rs550659379 | 0.882 | 0.160 | 5 | 143399780 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 5 |