Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1129055 | 0.724 | 0.400 | 3 | 122119472 | missense variant | G/A | snv | 0.30 | 0.25 | 15 | |
rs17281995 | 0.763 | 0.360 | 3 | 122120794 | 3 prime UTR variant | G/A;C | snv | 11 | |||
rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 131 | |
rs1805192 | 0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv | 121 | |||
rs7015626 | 1.000 | 0.120 | 8 | 124864572 | intron variant | G/A | snv | 0.39 | 1 | ||
rs2980874 | 0.925 | 0.120 | 8 | 125432546 | intron variant | G/A | snv | 0.30 | 2 | ||
rs2235108 | 0.925 | 0.120 | 8 | 125436547 | 3 prime UTR variant | G/A | snv | 0.25 | 3 | ||
rs2980879 | 0.925 | 0.120 | 8 | 125469233 | intron variant | A/T | snv | 0.69 | 3 | ||
rs752967378 | 0.882 | 0.160 | 3 | 12618580 | missense variant | G/A;C | snv | 4.0E-06 | 3 | ||
rs2066827 | 0.695 | 0.320 | 12 | 12718165 | missense variant | T/A;C;G | snv | 1.6E-04; 1.6E-05; 0.26 | 21 | ||
rs1561927 | 0.807 | 0.280 | 8 | 128555832 | intron variant | C/T | snv | 0.65 | 6 | ||
rs2736100 | 0.550 | 0.880 | 5 | 1286401 | 3 prime UTR variant | C/A | snv | 0.52 | 83 | ||
rs141095230 | 0.925 | 0.120 | 10 | 129536277 | missense variant | C/A;T | snv | 8.0E-06; 5.2E-05 | 2 | ||
rs12917 | 0.605 | 0.480 | 10 | 129708019 | missense variant | C/T | snv | 0.14 | 0.14 | 45 | |
rs2308321 | 0.653 | 0.480 | 10 | 129766800 | missense variant | A/G | snv | 9.3E-02 | 8.7E-02 | 29 | |
rs36115365 | 0.807 | 0.160 | 5 | 1313127 | upstream gene variant | G/A;C;T | snv | 7 | |||
rs401681 | 0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 | 42 | ||
rs488087 | 0.925 | 0.120 | 9 | 133071212 | synonymous variant | C/A;T | snv | 0.11 | 0.26 | 2 | |
rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 34 | |||
rs3124761 | 0.925 | 0.120 | 9 | 133474633 | intron variant | T/C | snv | 0.80 | 2 | ||
rs12456874 | 0.925 | 0.120 | 18 | 13366863 | intron variant | A/G | snv | 0.20 | 2 | ||
rs9502893 | 0.827 | 0.120 | 6 | 1339954 | intergenic variant | C/G;T | snv | 5 | |||
rs1235228469 | 0.925 | 0.120 | 3 | 138684714 | missense variant | C/A | snv | 8.0E-06 | 2 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 |