Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3917356 | 0.882 | 0.160 | 2 | 112834786 | intron variant | C/T | snv | 0.39 | 4 | ||
rs6720283 | 0.882 | 0.120 | 2 | 237401239 | intron variant | G/A | snv | 0.31 | 4 | ||
rs9679162 | 0.882 | 0.120 | 2 | 31024648 | intron variant | G/T | snv | 0.48 | 4 | ||
rs11889031 | 1.000 | 0.080 | 2 | 203934671 | upstream gene variant | C/T | snv | 0.15 | 1 | ||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs752021744 | 0.689 | 0.440 | 3 | 138759306 | missense variant | T/C | snv | 1.2E-05 | 29 | ||
rs3816527 | 0.882 | 0.160 | 3 | 157437525 | missense variant | C/A | snv | 0.64 | 0.64 | 9 | |
rs2607775 | 0.807 | 0.160 | 3 | 14178595 | 5 prime UTR variant | C/G | snv | 0.42 | 0.43 | 8 | |
rs2228468 | 0.882 | 0.120 | 3 | 42865620 | missense variant | A/C;T | snv | 0.43; 8.3E-03 | 6 | ||
rs6762208 | 0.851 | 0.200 | 3 | 185613377 | missense variant | C/A;T | snv | 0.36; 1.2E-05 | 4 | ||
rs7628626 | 0.925 | 0.120 | 3 | 119525574 | 3 prime UTR variant | A/C | snv | 0.82 | 2 | ||
rs1187825488 | 1.000 | 0.080 | 3 | 75737670 | frameshift variant | TT/- | del | 7.9E-04 | 1 | ||
rs761797378 | 1.000 | 0.080 | 3 | 75737671 | missense variant | T/A | snv | 2.0E-05 | 2.0E-05 | 1 | |
rs2231142 | 0.583 | 0.680 | 4 | 88131171 | missense variant | G/C;T | snv | 4.0E-06; 0.12 | 56 | ||
rs2071559 | 0.667 | 0.680 | 4 | 55126199 | upstream gene variant | A/G | snv | 0.53 | 26 | ||
rs11730582 | 0.807 | 0.240 | 4 | 87975269 | non coding transcript exon variant | T/C | snv | 0.37 | 10 | ||
rs13140012 | 0.827 | 0.320 | 4 | 186544404 | intron variant | T/A | snv | 0.41 | 6 | ||
rs2622621 | 0.851 | 0.240 | 4 | 88109768 | intron variant | C/A;G | snv | 6 | |||
rs4693608 | 0.827 | 0.200 | 4 | 83320204 | intron variant | G/A;C | snv | 6 | |||
rs11099592 | 0.851 | 0.160 | 4 | 83309466 | missense variant | T/C | snv | 0.78 | 0.80 | 5 | |
rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 58 | |
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 52 | |
rs11064 | 0.807 | 0.120 | 5 | 119393693 | 3 prime UTR variant | A/G | snv | 0.27 | 9 | ||
rs10053538 | 0.807 | 0.160 | 5 | 157110499 | intron variant | C/A;T | snv | 7 | |||
rs4705341 | 0.882 | 0.120 | 5 | 149426373 | non coding transcript exon variant | A/G | snv | 0.13 | 3 |