Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9275245 | 0.925 | 0.160 | 6 | 32693166 | intergenic variant | A/G;T | snv | 2 | |||
rs10498070 | 0.925 | 0.080 | 2 | 219833404 | intergenic variant | A/C | snv | 0.39 | 1 | ||
rs10499197 | 0.925 | 0.080 | 6 | 137811379 | intergenic variant | T/G | snv | 2.4E-02 | 1 | ||
rs11117432 | 0.851 | 0.200 | 16 | 85985665 | upstream gene variant | G/A | snv | 0.15 | 1 | ||
rs11642873 | 0.851 | 0.280 | 16 | 85958099 | intergenic variant | A/C | snv | 0.15 | 1 | ||
rs12711490 | 0.925 | 0.080 | 16 | 85939422 | intron variant | T/C | snv | 0.18 | 1 | ||
rs3131917 | 0.882 | 0.080 | 5 | 173230018 | upstream gene variant | T/G | snv | 0.52 | 1 | ||
rs35705950 | 0.763 | 0.240 | 11 | 1219991 | splice region variant | G/A;T | snv | 1 | |||
rs4342938 | 1.000 | 0.040 | 10 | 131557214 | intergenic variant | A/G | snv | 0.41 | 1 | ||
rs58721818 | 0.851 | 0.160 | 6 | 137922602 | regulatory region variant | C/G;T | snv | 1 | |||
rs624988 | 0.925 | 0.120 | 1 | 116721168 | regulatory region variant | T/A;C | snv | 1 | |||
rs6832151 | 0.925 | 0.160 | 4 | 40301616 | intergenic variant | G/A;T | snv | 1 | |||
rs7172677 | 0.925 | 0.080 | 15 | 75132252 | intergenic variant | A/C | snv | 0.71 | 1 | ||
rs924080 | 0.882 | 0.240 | 1 | 67294457 | intergenic variant | T/C | snv | 0.45 | 1 | ||
rs1035798 | 1.000 | 0.040 | 6 | 32183445 | splice region variant | G/A | snv | 0.24 | 0.19 | 1 | |
rs1535001 | 0.925 | 0.080 | 6 | 34959503 | intron variant | A/G | snv | 0.47 | 1 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
rs3827644 | 0.925 | 0.080 | 6 | 106237320 | intron variant | G/C | snv | 0.15 | 1 | ||
rs661968 | 1.000 | 0.040 | 15 | 33968868 | 5 prime UTR variant | C/T | snv | 0.80 | 1 | ||
rs10516487 | 0.752 | 0.360 | 4 | 101829919 | missense variant | G/A;T | snv | 0.26; 8.0E-06 | 2 | ||
rs17266594 | 0.807 | 0.280 | 4 | 101829765 | intron variant | T/C | snv | 0.25 | 0.27 | 1 | |
rs13277113 | 0.695 | 0.520 | 8 | 11491677 | intron variant | G/A | snv | 0.25 | 2 | ||
rs2409781 | 0.925 | 0.120 | 8 | 11502048 | intron variant | T/A;C | snv | 1 | |||
rs2904880 | 1.000 | 0.040 | 16 | 28933075 | missense variant | C/G | snv | 0.72 | 0.76 | 2 | |
rs763361 | 0.689 | 0.520 | 18 | 69864406 | missense variant | T/A;C | snv | 4.0E-06; 0.52 | 4 |