Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2523554 | 0.925 | 0.080 | 6 | 31364052 | upstream gene variant | C/T | snv | 0.70 | 5 | ||
rs12711490 | 0.925 | 0.080 | 16 | 85939422 | intron variant | T/C | snv | 0.18 | 4 | ||
rs2066807 | 0.925 | 0.080 | 12 | 56346898 | missense variant | C/G | snv | 4.9E-02 | 4.6E-02 | 4 | |
rs638893 | 0.882 | 0.080 | 11 | 118827828 | intergenic variant | G/A | snv | 0.79 | 4 | ||
rs10276619 | 1.000 | 0.080 | 7 | 50273756 | downstream gene variant | G/A | snv | 0.59 | 3 | ||
rs13239597 | 0.882 | 0.080 | 7 | 129055929 | non coding transcript exon variant | C/A | snv | 9.0E-02 | 3 | ||
rs2227513 | 1.000 | 0.080 | 12 | 68253559 | intron variant | T/C | snv | 0.15 | 3 | ||
rs2280381 | 0.882 | 0.080 | 16 | 85985027 | intron variant | C/T | snv | 0.64 | 3 | ||
rs2732552 | 0.925 | 0.080 | 11 | 35063045 | regulatory region variant | T/C | snv | 0.51 | 3 | ||
rs428073 | 1.000 | 0.080 | 12 | 118244946 | missense variant | C/G;T | snv | 0.72 | 3 | ||
rs6914831 | 1.000 | 0.080 | 6 | 135318506 | 3 prime UTR variant | C/T | snv | 0.59 | 0.59 | 3 | |
rs6932056 | 0.925 | 0.080 | 6 | 137921300 | intergenic variant | T/C | snv | 3.4E-02 | 3 | ||
rs77583790 | 0.882 | 0.080 | 3 | 159976265 | intron variant | G/A;C | snv | 3 | |||
rs7897633 | 1.000 | 0.080 | 10 | 51197961 | intron variant | C/A | snv | 0.64 | 3 | ||
rs9373839 | 0.882 | 0.080 | 6 | 106207742 | intron variant | T/C | snv | 0.15 | 3 | ||
rs10245867 | 0.925 | 0.080 | 7 | 28102567 | intron variant | G/T | snv | 0.37 | 2 | ||
rs1028488 | 1.000 | 0.080 | 6 | 170281387 | upstream gene variant | G/T | snv | 0.46 | 2 | ||
rs10498070 | 0.925 | 0.080 | 2 | 219833404 | intergenic variant | A/C | snv | 0.39 | 2 | ||
rs10499197 | 0.925 | 0.080 | 6 | 137811379 | intergenic variant | T/G | snv | 2.4E-02 | 2 | ||
rs10865035 | 1.000 | 0.080 | 2 | 100219272 | intron variant | A/G | snv | 0.42 | 2 | ||
rs1133906 | 0.925 | 0.080 | 7 | 93135669 | synonymous variant | C/T | snv | 0.22 | 0.28 | 2 | |
rs11755393 | 1.000 | 0.080 | 6 | 34856859 | missense variant | A/G;T | snv | 0.36 | 2 | ||
rs121909581 | 0.925 | 0.080 | 1 | 22639291 | stop gained | C/T | snv | 3.6E-05 | 2 | ||
rs14024 | 0.925 | 0.080 | 12 | 52675230 | missense variant | T/C | snv | 0.31 | 0.24 | 2 | |
rs140490 | 1.000 | 0.080 | 22 | 21567397 | intron variant | G/A;C;T | snv | 2 |