Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10484554 | 0.807 | 0.200 | 6 | 31306778 | intron variant | C/T | snv | 0.12 | 8 | ||
rs2247056 | 0.882 | 0.160 | 6 | 31297713 | intron variant | T/C | snv | 0.80 | 8 | ||
rs6457374 | 0.851 | 0.200 | 6 | 31304484 | intron variant | C/T | snv | 0.81 | 7 | ||
rs2156875 | 0.882 | 0.200 | 6 | 31349570 | intron variant | C/T | snv | 0.50 | 6 | ||
rs6906846 | 0.851 | 0.280 | 6 | 31277959 | non coding transcript exon variant | A/G | snv | 0.67 | 6 | ||
rs2894207 | 0.882 | 0.160 | 6 | 31295974 | intron variant | T/C | snv | 0.20 | 6 | ||
rs9366778 | 0.925 | 0.120 | 6 | 31301396 | intron variant | G/A | snv | 0.47 | 6 | ||
rs9264942 | 0.763 | 0.400 | 6 | 31306603 | intron variant | T/C | snv | 0.34 | 6 | ||
rs1058026 | 0.925 | 0.120 | 6 | 31353908 | 3 prime UTR variant | A/C | snv | 0.21 | 5 | ||
rs12191877 | 0.851 | 0.120 | 6 | 31285148 | intron variant | C/T | snv | 0.12 | 5 | ||
rs2523619 | 0.925 | 0.120 | 6 | 31350367 | intron variant | T/C | snv | 0.23 | 5 | ||
rs2844615 | 1.000 | 6 | 31275182 | intron variant | C/T | snv | 0.11 | 5 | |||
rs3819299 | 1.000 | 6 | 31354590 | non coding transcript exon variant | T/G | snv | 7.7E-02 | 2.3E-02 | 5 | ||
rs4386816 | 0.925 | 0.120 | 6 | 31279358 | intron variant | T/C | snv | 0.17 | 5 | ||
rs4394275 | 0.925 | 0.120 | 6 | 31350400 | intron variant | G/A | snv | 0.27 | 5 | ||
rs7382297 | 0.925 | 0.080 | 6 | 31279290 | intron variant | T/C;G | snv | 5 | |||
rs9265882 | 0.925 | 0.040 | 6 | 31345324 | intron variant | T/C | snv | 0.35 | 5 | ||
rs2249742 | 0.925 | 0.120 | 6 | 31272944 | intron variant | C/T | snv | 0.50 | 5 | ||
rs2395471 | 0.925 | 0.120 | 6 | 31272915 | intron variant | G/A | snv | 0.47 | 5 | ||
rs7759127 | 0.925 | 0.040 | 6 | 31273211 | intron variant | T/G | snv | 0.11 | 5 | ||
rs2524123 | 0.925 | 0.040 | 6 | 31297537 | intron variant | T/C | snv | 0.34 | 5 | ||
rs3873379 | 0.925 | 0.120 | 6 | 31294392 | intron variant | T/C | snv | 0.35 | 5 | ||
rs9380238 | 1.000 | 6 | 31299841 | intron variant | A/G | snv | 0.15 | 5 | |||
rs2523608 | 0.925 | 0.040 | 6 | 31354782 | non coding transcript exon variant | G/A | snv | 0.19 | 5 | ||
rs2394963 | 1.000 | 6 | 31283685 | intron variant | C/T | snv | 0.35 | 4 |