Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7717457 | 5 | 40887679 | intergenic variant | A/G | snv | 0.23 | 1 | ||||
rs776225963 | 19 | 35555490 | missense variant | G/A;T | snv | 1.1E-04 | 1 | ||||
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 | ||||
rs776968306 | 6 | 167024793 | missense variant | C/T | snv | 4.0E-06 | 1 | ||||
rs2237306 | 7 | 24717583 | intron variant | C/A;G;T | snv | 1 | |||||
rs201894482 | 5 | 138557977 | missense variant | G/A | snv | 6.0E-05 | 2.1E-05 | 1 | |||
rs1261963959 | 1 | 10297069 | missense variant | G/A | 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 | |||||
rs769394388 | 20 | 44355829 | missense variant | G/A;T | snv | 1 | |||||
rs169724 | 9 | 90828217 | intron variant | T/C;G | snv | 1 | |||||
rs182361 | 9 | 90828077 | intron variant | C/A | snv | 0.11 | 1 | ||||
rs771939956 | 17 | 7670705 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |||
rs1453340173 | 18 | 75286531 | missense variant | C/T | snv | 4.0E-06 | 1 | ||||
rs1372834410 | 3 | 11558705 | missense variant | C/T | snv | 1 | |||||
rs17227424 | 16 | 89738216 | missense variant | G/A;C | snv | 1.3E-05; 3.6E-02 | 1 | ||||
rs397509039 | 1.000 | 0.200 | 17 | 43092379 | missense variant | G/A;C | snv | 2 | |||
rs587781351 | 1.000 | 0.040 | 16 | 68828263 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs866551255 | 1.000 | 0.040 | 6 | 36684145 | missense variant | G/A | snv | 2 | |||
rs1390902532 | 1.000 | 0.040 | 9 | 21968766 | missense variant | T/C | snv | 7.4E-06 | 7.0E-06 | 2 | |
rs1356083197 | 1.000 | 0.040 | 1 | 224434068 | missense variant | C/T | snv | 1.5E-05 | 1.4E-05 | 2 | |
rs373646414 | 1.000 | 0.080 | 14 | 95132574 | missense variant | T/C | snv | 1.6E-05 | 5.6E-05 | 2 | |
rs2279398 | 1.000 | 0.080 | 5 | 177503768 | 3 prime UTR variant | C/T | snv | 2.7E-02 | 2 | ||
rs1457127715 | 17 | 39715810 | missense variant | G/A;C | snv | 4.0E-06 | 2 |