Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12363415 | 1.000 | 0.080 | 11 | 13377061 | intron variant | A/G | snv | 0.20 | 1 | ||
rs2073746 | 1.000 | 0.080 | 22 | 19991035 | intron variant | T/C | snv | 0.80 | 1 | ||
rs4901043 | 1.000 | 0.080 | 14 | 50616876 | intron variant | T/C | snv | 0.49 | 1 | ||
rs16980013 | 1.000 | 0.080 | 19 | 45764195 | 3 prime UTR variant | G/T | snv | 0.24 | 1 | ||
rs754107 | 1.000 | 0.080 | 2 | 127103254 | intron variant | C/G | snv | 0.63 | 1 | ||
rs17512204 | 1.000 | 0.080 | 2 | 117975255 | missense variant | G/A | snv | 5.6E-02 | 5.3E-02 | 1 | |
rs2233872 | 1.000 | 0.080 | 9 | 34691559 | upstream gene variant | A/G | snv | 0.21 | 1 | ||
rs11574915 | 1.000 | 0.080 | 9 | 34710087 | 5 prime UTR variant | A/C;G | snv | 0.13; 4.1E-06 | 1 | ||
rs17237890 | 1.000 | 0.080 | 16 | 56962246 | 5 prime UTR variant | T/C | snv | 1 | |||
rs1800774 | 1.000 | 0.080 | 16 | 56981633 | intron variant | C/A;T | snv | 4.0E-06; 0.32; 4.0E-06 | 1 | ||
rs942576 | 1.000 | 0.080 | 10 | 69903027 | intron variant | G/T | snv | 0.30 | 1 | ||
rs55940034 | 1.000 | 0.080 | 13 | 110390962 | intron variant | A/G | snv | 0.28 | 1 | ||
rs2434237 | 1.000 | 0.080 | 5 | 175797902 | intron variant | C/A | snv | 0.18 | 1 | ||
rs4407312 | 1.000 | 0.080 | 20 | 23826391 | intron variant | A/C;G;T | snv | 0.76; 4.1E-06; 6.6E-05 | 1 | ||
rs6048952 | 1.000 | 0.080 | 20 | 23626620 | downstream gene variant | A/G | snv | 0.27 | 1 | ||
rs1276663775 | 1.000 | 0.080 | 20 | 23879610 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
rs9462875 | 1.000 | 0.080 | 6 | 43200379 | intron variant | A/G | snv | 0.24 | 1 | ||
rs1050998 | 1.000 | 0.080 | 17 | 4735442 | missense variant | A/G | snv | 0.46 | 0.41 | 1 | |
rs8123 | 1.000 | 0.080 | 17 | 4733270 | 3 prime UTR variant | T/G | snv | 0.22 | 1 | ||
rs6723449 | 1.000 | 0.080 | 2 | 218132857 | intron variant | T/C | snv | 0.62 | 1 | ||
rs1058932 | 1.000 | 0.080 | 10 | 95037104 | 3 prime UTR variant | G/A | snv | 0.22 | 0.24 | 1 | |
rs10889160 | 1.000 | 0.080 | 1 | 59896449 | intron variant | T/C | snv | 0.23 | 1 | ||
rs2271800 | 1.000 | 0.080 | 1 | 59907994 | intron variant | A/C;T | snv | 1 | |||
rs3093200 | 1.000 | 0.080 | 19 | 15878779 | missense variant | G/C;T | snv | 5.3E-02 | 1 | ||
rs669173 | 1.000 | 0.080 | 1 | 85433745 | intron variant | T/C | snv | 0.42 | 1 |