Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1018379423 | 1 | 22907986 | missense variant | G/T | snv | 4.0E-06 | 2.1E-05 | 4 | |||
rs863224683 | 17 | 7675224 | missense variant | G/A;C | snv | 4 | |||||
rs74751600 | 22 | 28695852 | missense variant | T/C | snv | 3 | |||||
rs778826879 | 16 | 30121948 | missense variant | C/G;T | snv | 1.2E-05; 8.0E-06 | 3 | ||||
rs1457127715 | 17 | 39715810 | missense variant | G/A;C | snv | 4.0E-06 | 2 | ||||
rs587776946 | 1.000 | 1 | 113114471 | stop gained | C/T | snv | 2 | ||||
rs72478580 | 1.000 | 5 | 35072610 | missense variant | T/G | snv | 1.9E-02 | 1.9E-02 | 2 | ||
rs751478142 | 1.000 | 5 | 138570994 | missense variant | G/A | snv | 2.8E-05 | 1.4E-05 | 2 | ||
rs753066745 | X | 81277164 | missense variant | C/T | snv | 1.7E-05 | 9.5E-06 | 2 | |||
rs771308693 | 8 | 140752306 | missense variant | G/A | snv | 3.2E-05 | 7.0E-06 | 2 | |||
rs1051992 | 11 | 6319476 | missense variant | A/G | snv | 4.2E-06; 0.55 | 0.51 | 1 | |||
rs11646171 | 16 | 61824185 | intron variant | G/A | snv | 0.13 | 1 | ||||
rs1261963959 | 1 | 10297069 | missense variant | G/A | snv | 4.0E-06 | 1 | ||||
rs1372834410 | 3 | 11558705 | missense variant | C/T | snv | 1 | |||||
rs1453340173 | 18 | 75286531 | missense variant | C/T | snv | 4.0E-06 | 1 | ||||
rs148526538 | 12 | 52520269 | missense variant | G/A;C | snv | 8.9E-05; 4.0E-06 | 1 | ||||
rs1634507 | 17 | 36098180 | regulatory region variant | G/A;T | snv | 1 | |||||
rs169724 | 9 | 90828217 | intron variant | T/C;G | snv | 1 | |||||
rs17227424 | 16 | 89738216 | missense variant | G/A;C | snv | 1.3E-05; 3.6E-02 | 1 | ||||
rs182361 | 9 | 90828077 | intron variant | C/A | snv | 0.11 | 1 | ||||
rs201894482 | 5 | 138557977 | missense variant | G/A | snv | 6.0E-05 | 2.1E-05 | 1 | |||
rs2237306 | 7 | 24717583 | intron variant | C/A;G;T | snv | 1 | |||||
rs769394388 | 20 | 44355829 | missense variant | G/A;T | snv | 1 | |||||
rs7717457 | 5 | 40887679 | intergenic variant | A/G | snv | 0.23 | 1 | ||||
rs771939956 | 17 | 7670705 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 |