Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 16 | ||
rs11014166 | 0.882 | 0.040 | 10 | 18419869 | intron variant | A/T | snv | 0.27 | 10 | ||
rs5880 | 0.827 | 0.040 | 16 | 56981179 | missense variant | G/C | snv | 5.2E-02 | 3.7E-02 | 10 | |
rs2001844 | 0.882 | 0.040 | 8 | 125466503 | upstream gene variant | A/G | snv | 0.43 | 9 | ||
rs2144300 | 0.882 | 0.040 | 1 | 230159169 | intron variant | C/T | snv | 0.44 | 7 | ||
rs216311 | 0.882 | 0.040 | 12 | 6019277 | missense variant | T/A;C | snv | 4.0E-06; 0.69 | 7 | ||
rs342293 | 0.882 | 0.040 | 7 | 106731773 | intron variant | C/G | snv | 0.42 | 7 | ||
rs2306235 | 0.827 | 0.040 | 1 | 150150942 | missense variant | C/G;T | snv | 1.1E-02; 1.6E-05 | 4.4E-03 | 6 | |
rs3900940 | 0.827 | 0.040 | 3 | 108428881 | missense variant | T/A;C | snv | 4.3E-06; 0.24 | 6 | ||
rs11057830 | 0.851 | 0.040 | 12 | 124822507 | intron variant | G/A | snv | 0.15 | 5 | ||
rs1384889210 | 0.827 | 0.040 | 11 | 116836193 | missense variant | C/A | snv | 5 | |||
rs2298566 | 0.827 | 0.040 | 11 | 130880747 | missense variant | A/C;T | snv | 0.77; 4.0E-06 | 5 | ||
rs3828599 | 0.882 | 0.040 | 5 | 151022235 | intron variant | A/G | snv | 0.67 | 5 | ||
rs763802417 | 0.882 | 0.040 | X | 100862805 | missense variant | G/A | snv | 5.9E-06 | 5 | ||
rs9332978 | 0.882 | 0.040 | 1 | 46942278 | upstream gene variant | T/C | snv | 7.3E-02 | 5 | ||
rs1058930 | 0.882 | 0.040 | 10 | 95058362 | missense variant | G/A;C | snv | 1.0E-04; 3.7E-02 | 4 | ||
rs116092985 | 0.882 | 0.040 | 16 | 2110972 | missense variant | A/G | snv | 6.5E-02 | 7.8E-02 | 4 | |
rs1199475313 | 0.851 | 0.040 | 8 | 37966277 | missense variant | T/C | snv | 7.0E-06 | 4 | ||
rs13144478 | 0.882 | 0.040 | 4 | 115275150 | regulatory region variant | A/T | snv | 5.5E-02 | 4 | ||
rs142677199 | 0.882 | 0.040 | 17 | 63479897 | missense variant | G/A;T | snv | 3.2E-05 | 4 | ||
rs1790349 | 0.882 | 0.040 | 11 | 71431304 | intron variant | T/C | snv | 0.19 | 4 | ||
rs180070 | 0.882 | 0.040 | 17 | 69960745 | upstream gene variant | G/T | snv | 0.77 | 4 | ||
rs2015086 | 0.882 | 0.040 | 17 | 36064257 | upstream gene variant | A/G | snv | 0.22 | 4 | ||
rs3931020 | 0.882 | 0.040 | 1 | 74769633 | downstream gene variant | T/C | snv | 0.71 | 4 | ||
rs4888378 | 0.851 | 0.040 | 16 | 75298143 | intron variant | A/G | snv | 0.52 | 4 |