Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9727115 | 1 | 98711697 | intron variant | G/A | snv | 0.37 | 1 | ||||
rs2943641 | 0.763 | 0.160 | 2 | 226229029 | intergenic variant | T/C | snv | 0.67 | 18 | ||
rs6235 | 0.925 | 0.120 | 5 | 96393194 | missense variant | C/G | snv | 0.26 | 0.23 | 8 | |
rs742642 | 1.000 | 0.080 | 6 | 20664850 | intron variant | G/A | snv | 0.21 | 3 | ||
rs6930337 | 6 | 148466870 | intron variant | C/G;T | snv | 1 | |||||
rs933360 | 7 | 50690548 | intron variant | C/T | snv | 0.60 | 2 | ||||
rs11558471 | 1.000 | 0.080 | 8 | 117173494 | 3 prime UTR variant | A/G | snv | 0.25 | 5 | ||
rs3824420 | 9 | 712766 | missense variant | G/A;C | snv | 3.8E-02; 1.2E-05 | 1 | ||||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 93 | |||
rs5015480 | 0.851 | 0.120 | 10 | 92705802 | downstream gene variant | C/T | snv | 0.42 | 9 | ||
rs11185790 | 10 | 89612776 | intron variant | G/A | snv | 0.15 | 3 | ||||
rs10830963 | 0.776 | 0.400 | 11 | 92975544 | intron variant | C/G | snv | 0.22 | 27 | ||
rs10501320 | 0.925 | 0.120 | 11 | 47272248 | 5 prime UTR variant | G/C | snv | 0.17 | 5 | ||
rs11603334 | 1.000 | 0.080 | 11 | 72721940 | 5 prime UTR variant | G/A | snv | 0.12 | 5 | ||
rs7944584 | 1.000 | 0.080 | 11 | 47314769 | intron variant | A/T | snv | 0.19 | 5 | ||
rs1051006 | 11 | 47285034 | missense variant | G/A;C | snv | 0.26; 4.0E-06 | 2 | ||||
rs10838687 | 11 | 47291341 | intron variant | T/G | snv | 0.31 | 2 | ||||
rs35233100 | 11 | 47285079 | stop gained | C/T | snv | 3.8E-02 | 3.9E-02 | 1 | |||
rs150781447 | 12 | 64830440 | missense variant | C/T | snv | 5.4E-03 | 5.3E-03 | 1 | |||
rs4502156 | 1.000 | 0.080 | 15 | 62090956 | intergenic variant | T/C | snv | 0.55 | 4 | ||
rs7172432 | 0.925 | 0.080 | 15 | 62104190 | intergenic variant | A/G | snv | 0.51 | 4 | ||
rs1549318 | 15 | 70816808 | intergenic variant | C/T | snv | 0.55 | 1 | ||||
rs4790333 | 17 | 2359409 | intron variant | C/A;T | snv | 0.44 | 1 | ||||
rs61741902 | 17 | 2379485 | missense variant | G/A | snv | 1.0E-02 | 9.1E-03 | 1 | |||
rs1800437 | 0.827 | 0.160 | 19 | 45678134 | missense variant | G/C | snv | 0.18 | 0.17 | 13 |