Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6932730 | 0.925 | 6 | 31386405 | upstream gene variant | T/C | snv | 0.26 | 5 | |||
rs17616434 | 1.000 | 4 | 38811255 | intron variant | T/C | snv | 0.44 | 2 | |||
rs9865818 | 1.000 | 3 | 188354725 | intron variant | A/G | snv | 0.34 | 2 | |||
rs71625199 | 1.000 | 1 | 152307488 | synonymous variant | C/A;T | snv | 8.0E-06; 2.3E-02 | 1 | |||
rs17454584 | 0.851 | 0.080 | 4 | 122432277 | downstream gene variant | A/G | snv | 0.17 | 6 | ||
rs10056340 | 0.925 | 0.080 | 5 | 110854353 | intergenic variant | T/G | snv | 0.31 | 3 | ||
rs3771175 | 0.925 | 0.080 | 2 | 102343750 | 3 prime UTR variant | T/A | snv | 0.18 | 3 | ||
rs4742170 | 0.925 | 0.080 | 9 | 6242950 | intron variant | C/G;T | snv | 3 | |||
rs4410871 | 0.925 | 0.080 | 8 | 127802783 | intron variant | T/C | snv | 0.74 | 2 | ||
rs769790595 | 0.827 | 0.120 | 16 | 27360785 | missense variant | G/A;C | snv | 2.0E-05; 4.0E-06 | 5 | ||
rs2251746 | 0.882 | 0.120 | 1 | 159302270 | intron variant | T/C | snv | 0.20 | 3 | ||
rs2427837 | 0.851 | 0.160 | 1 | 159288755 | upstream gene variant | G/A | snv | 0.20 | 5 | ||
rs447713 | 0.851 | 0.160 | 2 | 113130095 | non coding transcript exon variant | A/G | snv | 0.21 | 5 | ||
rs13222905 | 0.882 | 0.160 | 7 | 150566901 | upstream gene variant | G/A | snv | 0.15 | 3 | ||
rs6965571 | 0.882 | 0.160 | 7 | 150737384 | 5 prime UTR variant | G/A | snv | 0.18 | 3 | ||
rs2289278 | 0.827 | 0.200 | 5 | 111073450 | 5 prime UTR variant | C/G | snv | 8.7E-02 | 5 | ||
rs1059513 | 0.776 | 0.240 | 12 | 57095926 | 3 prime UTR variant | T/C | snv | 8.0E-02 | 11 | ||
rs2155219 | 0.732 | 0.280 | 11 | 76588150 | upstream gene variant | G/T | snv | 0.52 | 14 | ||
rs6906021 | 0.827 | 0.320 | 6 | 32658534 | upstream gene variant | T/C | snv | 0.47 | 6 | ||
rs8034191 | 0.695 | 0.440 | 15 | 78513681 | intron variant | T/C | snv | 0.27 | 24 | ||
rs555743307 | 0.695 | 0.440 | 16 | 27342243 | missense variant | G/A;T | snv | 3.6E-05; 2.9E-04 | 20 | ||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs2569190 | 0.620 | 0.560 | 5 | 140633331 | intron variant | A/G | snv | 0.57 | 39 | ||
rs1042714 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 54 | ||
rs1801275 | 0.581 | 0.680 | 16 | 27363079 | missense variant | A/G | snv | 0.25 | 0.36 | 58 |