Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7758229 | 0.732 | 0.120 | 6 | 160419220 | intron variant | G/A;T | snv | 16 | |||
rs1179251 | 0.763 | 0.320 | 12 | 68251271 | intron variant | C/G | snv | 0.18 | 14 | ||
rs1284806277 | 0.827 | 0.200 | 14 | 102251978 | missense variant | A/G | snv | 1.4E-05 | 13 | ||
rs77191406 | 0.790 | 0.280 | 6 | 137881704 | 3 prime UTR variant | C/T | snv | 7.2E-04 | 12 | ||
rs992157 | 0.790 | 0.080 | 2 | 218290058 | 5 prime UTR variant | G/A | snv | 0.46 | 10 | ||
rs28929495 | 0.807 | 0.120 | 7 | 55174014 | missense variant | G/A;C;T | snv | 9 | |||
rs629849 | 0.827 | 0.160 | 6 | 160073377 | missense variant | A/C;G;T | snv | 0.90 | 0.91 | 9 | |
rs2555639 | 0.851 | 0.080 | 4 | 174540379 | non coding transcript exon variant | T/C | snv | 0.38 | 7 | ||
rs60745952 | 0.925 | 0.080 | 4 | 148827842 | intron variant | T/C | snv | 0.13 | 6 | ||
rs35301225 | 0.882 | 0.080 | 1 | 9151743 | mature miRNA variant | C/A;T | snv | 5 | |||
rs3775292 | 0.851 | 0.080 | 4 | 186081871 | non coding transcript exon variant | C/G | snv | 0.82 | 5 |