Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2305480 | 0.763 | 0.280 | 17 | 39905943 | missense variant | G/A | snv | 0.40 | 0.35 | 7 | |
rs2290400 | 0.790 | 0.360 | 17 | 39909987 | intron variant | T/C | snv | 0.48 | 6 | ||
rs8067378 | 0.752 | 0.240 | 17 | 39895095 | regulatory region variant | A/G | snv | 0.50 | 6 | ||
rs11557467 | 0.851 | 0.200 | 17 | 39872381 | missense variant | G/T | snv | 0.45 | 0.45 | 4 | |
rs2305479 | 0.882 | 0.160 | 17 | 39905964 | missense variant | C/T | snv | 0.43 | 0.39 | 4 | |
rs7219923 | 0.882 | 0.160 | 17 | 39918265 | non coding transcript exon variant | C/T | snv | 0.52 | 4 | ||
rs9303277 | 0.790 | 0.240 | 17 | 39820216 | intron variant | C/T | snv | 0.52 | 4 | ||
rs9303281 | 0.882 | 0.160 | 17 | 39917793 | non coding transcript exon variant | G/A | snv | 0.50 | 4 | ||
rs3859192 | 0.925 | 0.080 | 17 | 39972395 | intron variant | C/T | snv | 0.42 | 3 | ||
rs4794820 | 0.790 | 0.160 | 17 | 39933091 | intron variant | A/G;T | snv | 3 | |||
rs4795400 | 0.925 | 0.080 | 17 | 39910767 | intron variant | C/T | snv | 0.36 | 3 | ||
rs4795405 | 0.851 | 0.160 | 17 | 39932164 | intron variant | T/A;C | snv | 3 | |||
rs8069176 | 0.882 | 0.080 | 17 | 39900944 | downstream gene variant | G/A;T | snv | 3 | |||
rs8076131 | 0.790 | 0.200 | 17 | 39924659 | intron variant | G/A;C | snv | 3 | |||
rs907092 | 0.925 | 0.080 | 17 | 39766006 | synonymous variant | G/A | snv | 0.41 | 0.36 | 3 | |
rs3894194 | 0.882 | 0.120 | 17 | 39965740 | missense variant | G/A | snv | 0.46 | 0.41 | 2 | |
rs3902025 | 0.925 | 0.080 | 17 | 39963001 | intron variant | G/T | snv | 0.56 | 2 | ||
rs4795408 | 0.925 | 0.080 | 17 | 39951374 | upstream gene variant | G/A | snv | 0.41 | 2 | ||
rs6503525 | 0.925 | 0.080 | 17 | 39938921 | intron variant | G/A;C | snv | 2 | |||
rs6503526 | 0.925 | 0.080 | 17 | 39958345 | intron variant | C/T | snv | 0.41 | 2 | ||
rs8079416 | 0.925 | 0.080 | 17 | 39936460 | intron variant | T/C | snv | 0.45 | 2 |