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
SYK
9 90828217 intron variant T/C;G snv 1
rs182361
SYK
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