Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11603334 | 1.000 | 0.080 | 11 | 72721940 | 5 prime UTR variant | G/A | snv | 0.12 | 4 | ||
rs7756992 | 0.827 | 0.240 | 6 | 20679478 | intron variant | A/G;T | snv | 4 | |||
rs1799884 | 1.000 | 0.080 | 7 | 44189469 | intron variant | C/T | snv | 0.17 | 4 | ||
rs10758593 | 0.827 | 0.240 | 9 | 4292083 | intron variant | G/A | snv | 0.45 | 4 | ||
rs780110 | 0.925 | 0.120 | 2 | 27462521 | intron variant | G/A | snv | 0.56 | 4 | ||
rs4402960 | 0.724 | 0.400 | 3 | 185793899 | intron variant | G/T | snv | 0.38 | 4 | ||
rs4665965 | 0.925 | 0.120 | 2 | 27313513 | intron variant | T/A;C | snv | 4 | |||
rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 4 | ||
rs17762454 | 0.925 | 0.120 | 6 | 7212967 | non coding transcript exon variant | C/T | snv | 0.25 | 4 | ||
rs4506565 | 0.790 | 0.280 | 10 | 112996282 | intron variant | A/G;T | snv | 4 | |||
rs13404446 | 0.925 | 0.120 | 2 | 27296386 | intron variant | G/A | snv | 0.42 | 4 | ||
rs10885122 | 1.000 | 0.080 | 10 | 111282335 | intergenic variant | T/G | snv | 0.71 | 3 | ||
rs11257655 | 1.000 | 0.080 | 10 | 12265895 | TF binding site variant | C/T | snv | 0.23 | 3 | ||
rs1483121 | 1.000 | 0.080 | 11 | 48311808 | downstream gene variant | G/A | snv | 9.7E-02 | 3 | ||
rs4502156 | 1.000 | 0.080 | 15 | 62090956 | intergenic variant | T/C | snv | 0.55 | 3 | ||
rs853789 | 2 | 168944978 | intron variant | A/G;T | snv | 0.75 | 3 | ||||
rs11717195 | 1.000 | 0.080 | 3 | 123363551 | intron variant | T/C | snv | 0.19 | 3 | ||
rs2877716 | 3 | 123375604 | intron variant | T/C | snv | 0.76 | 3 | ||||
rs1552224 | 1.000 | 0.080 | 11 | 72722053 | 5 prime UTR variant | A/C | snv | 0.12 | 3 | ||
rs9356744 | 0.882 | 0.120 | 6 | 20685255 | intron variant | T/C | snv | 0.42 | 3 | ||
rs11605924 | 1.000 | 0.080 | 11 | 45851540 | intron variant | A/C | snv | 0.39 | 3 | ||
rs17168486 | 1.000 | 0.080 | 7 | 14858657 | intron variant | C/T | snv | 0.18 | 3 | ||
rs1371614 | 2 | 26930006 | intron variant | C/T | snv | 0.29 | 3 | ||||
rs1783598 | 1.000 | 0.080 | 11 | 73140418 | intron variant | C/G;T | snv | 3 | |||
rs4607517 | 0.882 | 0.080 | 7 | 44196069 | intron variant | G/A;C | snv | 3 |