Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1042138 | 0.882 | 0.120 | 7 | 93426338 | 3 prime UTR variant | G/A | snv | 0.15 | 0.11 | 3 | |
rs1042636 | 0.672 | 0.360 | 3 | 122284922 | missense variant | A/G | snv | 0.15 | 9.0E-02 | 23 | |
rs1126616 | 0.827 | 0.280 | 4 | 87982701 | synonymous variant | C/G;T | snv | 0.32 | 0.26 | 8 | |
rs11746443 | 0.882 | 0.120 | 5 | 177371305 | intron variant | G/A | snv | 0.24 | 0.21 | 4 | |
rs1207568 | 0.925 | 0.120 | 13 | 33016046 | upstream gene variant | G/A | snv | 0.17 | 3 | ||
rs121907892 | 0.807 | 0.240 | 11 | 64593747 | stop gained | G/A;C | snv | 2.8E-04 | 8 | ||
rs121907896 | 0.851 | 0.200 | 11 | 64591825 | missense variant | G/A | snv | 1.8E-04 | 8.4E-05 | 5 | |
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs13006480 | 1.000 | 0.080 | 2 | 27764354 | intergenic variant | C/G;T | snv | 1 | |||
rs13041834 | 1.000 | 0.080 | 20 | 54086745 | intergenic variant | T/C | snv | 0.42 | 1 | ||
rs1544935 | 0.925 | 0.160 | 6 | 39156672 | intergenic variant | T/G | snv | 0.18 | 3 | ||
rs1801197 | 0.851 | 0.240 | 7 | 93426441 | missense variant | A/G | snv | 0.39 | 0.36 | 5 | |
rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 39 | |
rs1801726 | 0.732 | 0.280 | 3 | 122284985 | missense variant | G/C | snv | 0.95 | 0.92 | 13 | |
rs2079742 | 0.851 | 0.240 | 17 | 61388336 | non coding transcript exon variant | T/C | snv | 0.20 | 9 | ||
rs2286526 | 1.000 | 0.080 | 17 | 61394696 | non coding transcript exon variant | C/G;T | snv | 2 | |||
rs35747824 | 1.000 | 0.080 | 16 | 20381986 | intron variant | A/T | snv | 0.24 | 1 | ||
rs3798519 | 1.000 | 0.080 | 6 | 50821065 | intron variant | A/C;G | snv | 2 | |||
rs4236480 | 0.882 | 0.120 | 7 | 142929454 | missense variant | T/A;C;G | snv | 3 | |||
rs4236481 | 1.000 | 0.080 | 7 | 142929678 | intron variant | C/A;G | snv | 1 | |||
rs4252402 | 1.000 | 0.080 | 7 | 142930043 | intron variant | A/G | snv | 0.79 | 1 | ||
rs4252417 | 1.000 | 0.080 | 7 | 142928163 | synonymous variant | G/A | snv | 5.1E-02 | 9.2E-02 | 1 | |
rs6123359 | 1.000 | 0.080 | 20 | 54098167 | regulatory region variant | A/G | snv | 0.12 | 2 | ||
rs6667242 | 1.000 | 0.080 | 1 | 21500073 | intergenic variant | A/G | snv | 0.16 | 1 | ||
rs6928986 | 1.000 | 0.080 | 6 | 131002852 | intron variant | C/T | snv | 0.78 | 1 |