Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
rs1085307051 | 0.925 | 0.160 | 5 | 88883309 | 5 prime UTR variant | GAGGAGGAGGAAGA/- | del | 5 | |||
rs302668 | 0.925 | 0.120 | 11 | 88143743 | intron variant | T/C | snv | 0.28 | 2 | ||
rs4878104 | 0.851 | 0.120 | 9 | 87578076 | intron variant | C/T | snv | 0.40 | 4 | ||
rs4877365 | 0.851 | 0.120 | 9 | 87540777 | intron variant | G/A | snv | 0.28 | 4 | ||
rs981951447 | 0.925 | 0.120 | 5 | 87268726 | missense variant | C/T | snv | 2 | |||
rs78268395 | 1.000 | 0.120 | 3 | 87253740 | missense variant | G/A | snv | 1.5E-03 | 6.9E-03 | 1 | |
rs72824905 | 0.827 | 0.200 | 16 | 81908423 | missense variant | C/G;T | snv | 5.2E-03 | 6 | ||
rs2255166 | 1.000 | 0.120 | 17 | 81239762 | non coding transcript exon variant | T/C | snv | 0.37 | 1 | ||
rs1048775 | 1.000 | 0.120 | 17 | 81228529 | 3 prime UTR variant | G/C | snv | 0.42 | 1 | ||
rs969413 | 1.000 | 0.120 | 17 | 81222014 | intron variant | T/A | snv | 0.39 | 1 | ||
rs9319617 | 1.000 | 0.120 | 17 | 81218646 | intron variant | T/C | snv | 0.47 | 1 | ||
rs2725391 | 1.000 | 0.120 | 17 | 81218630 | intron variant | C/T | snv | 0.37 | 1 | ||
rs2659030 | 1.000 | 0.120 | 17 | 81204174 | intron variant | G/A;T | snv | 0.36 | 1 | ||
rs906175 | 1.000 | 0.120 | 17 | 81199662 | non coding transcript exon variant | C/T | snv | 0.37 | 1 | ||
rs7240419 | 1.000 | 0.120 | 18 | 79168989 | intron variant | G/A | snv | 0.24 | 1 | ||
rs1401496725 | 0.925 | 0.120 | 2 | 79121657 | missense variant | C/G;T | snv | 8.0E-06; 8.0E-06 | 2 | ||
rs544706237 | 0.851 | 0.120 | 2 | 79121649 | missense variant | A/G;T | snv | 8.0E-06; 5.2E-05 | 5 | ||
rs1205185774 | 0.882 | 0.120 | 14 | 77469161 | missense variant | C/T | snv | 4 | |||
rs6962939 | 1.000 | 0.120 | 7 | 7484595 | intron variant | T/A | snv | 5.4E-02 | 1 | ||
rs121909345 | 0.882 | 0.120 | 2 | 74363337 | missense variant | C/T | snv | 2.8E-05 | 2.1E-05 | 4 | |
rs63750083 | 0.732 | 0.160 | 14 | 73219177 | missense variant | C/A;T | snv | 13 | |||
rs63751223 | 0.807 | 0.160 | 14 | 73219161 | missense variant | G/C | snv | 6 | |||
rs661 | 0.807 | 0.120 | 14 | 73217225 | missense variant | G/A;T | snv | 4.0E-06 | 6 | ||
rs1566650594 | 0.851 | 0.120 | 14 | 73206384 | splice acceptor variant | A/T | snv | 4 |