Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2010963 | 0.542 | 0.840 | 6 | 43770613 | 5 prime UTR variant | C/G | snv | 0.68 | 82 | ||
rs3025039 | 0.576 | 0.720 | 6 | 43784799 | 3 prime UTR variant | C/T | snv | 0.13 | 62 | ||
rs1982073 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 32 | |||
rs12976445 | 0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 | 20 | ||
rs2868371 | 0.827 | 0.120 | 7 | 76301442 | upstream gene variant | C/G | snv | 0.22 | 6 | ||
rs3757 | 0.851 | 0.160 | 22 | 20111808 | 3 prime UTR variant | G/A | snv | 0.21 | 5 | ||
rs587782477 | 0.882 | 0.120 | 5 | 112775679 | missense variant | A/T | snv | 4 | |||
rs1061285 | 0.925 | 0.120 | 7 | 129213467 | 3 prime UTR variant | C/A;G | snv | 2 | |||
rs720014 | 1.000 | 0.080 | 22 | 20111359 | 3 prime UTR variant | T/C | snv | 0.22 | 1 | ||
rs1217371203 | 0.882 | 0.120 | 3 | 122106342 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 4 | ||
rs1633445 | 0.925 | 0.120 | 22 | 20113073 | non coding transcript exon variant | T/A;C | snv | 1.2E-05; 0.23 | 2 | ||
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 |