Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10010325 | 1.000 | 0.040 | 4 | 105185196 | intron variant | C/A;G;T | snv | 1 | |||
rs10037512 | 5 | 89058858 | intron variant | T/A;C | snv | 1 | |||||
rs10058074 | 5 | 132350453 | intron variant | G/A | snv | 0.31 | 1 | ||||
rs1013209 | 8 | 24258791 | intergenic variant | C/T | snv | 0.28 | 1 | ||||
rs10152591 | 15 | 69755818 | intron variant | A/C | snv | 9.8E-02 | 1 | ||||
rs10187066 | 2 | 218650036 | intron variant | A/G | snv | 0.45 | 1 | ||||
rs10189857 | 1.000 | 0.080 | 2 | 60486100 | intron variant | A/G | snv | 0.42 | 2 | ||
rs10231759 | 7 | 150815084 | regulatory region variant | T/C | snv | 0.41 | 1 | ||||
rs1029534 | 7 | 28149464 | intron variant | T/C;G | snv | 1 | |||||
rs10401193 | 19 | 19480257 | intron variant | A/G | snv | 0.19 | 1 | ||||
rs1042725 | 0.882 | 0.080 | 12 | 65964567 | 3 prime UTR variant | C/T | snv | 0.48 | 2 | ||
rs1043515 | 17 | 38765943 | 3 prime UTR variant | A/G | snv | 0.46 | 1 | ||||
rs1046934 | 1.000 | 0.080 | 1 | 184054395 | missense variant | A/C;G;T | snv | 0.34; 4.0E-06 | 1 | ||
rs1046943 | 1.000 | 0.040 | 6 | 109462738 | 3 prime UTR variant | A/G | snv | 0.52 | 1 | ||
rs1047014 | 6 | 19841262 | 3 prime UTR variant | T/C | snv | 0.23 | 1 | ||||
rs10472828 | 5 | 32888712 | non coding transcript exon variant | C/T | snv | 0.40 | 1 | ||||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 8 | |
rs10492321 | 12 | 93586312 | downstream gene variant | T/A | snv | 0.20 | 1 | ||||
rs10512248 | 0.925 | 0.120 | 9 | 95497421 | intron variant | T/A;G | snv | 1 | |||
rs10513137 | 3 | 141424588 | intron variant | G/A;C | snv | 1 | |||||
rs10519170 | 15 | 48393978 | regulatory region variant | A/G | snv | 0.18 | 1 | ||||
rs1052483 | 2 | 219069626 | non coding transcript exon variant | G/T | snv | 0.13 | 1 | ||||
rs1074683 | 20 | 33716847 | intron variant | C/G | snv | 0.24 | 1 | ||||
rs10748128 | 12 | 69433878 | intergenic variant | G/T | snv | 0.42 | 1 | ||||
rs10770705 | 12 | 20704533 | intron variant | A/C | snv | 0.70 | 1 |