Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519825
BTK
0.882 0.120 X 101356176 missense variant C/G snv 1
rs1057519826
BTK
0.882 0.120 X 101356177 missense variant A/T snv 1
rs13114738 0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs6214 0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 1
rs11568818 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 2
rs3740393 0.776 0.280 10 102876898 intron variant G/C;T snv 1
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 2
rs3753841 0.827 0.080 1 102914362 missense variant G/A snv 0.61 0.49 3
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs314276 0.807 0.280 6 104960124 intron variant A/C snv 0.65 2
rs3018066 4 106368369 intron variant A/G;T snv 0.38 1
rs450533 4 106909104 intron variant T/C snv 0.36 1
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 4
rs587776551
ATM
1.000 0.200 11 108281168 missense variant G/A;T snv 1.6E-05 1.4E-05 2
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 3
rs564652222 0.925 0.280 11 108325416 missense variant C/A;T snv 1.4E-05 3
rs769142993 0.851 0.280 11 108331498 missense variant G/C;T snv 2.4E-05 7.0E-06 2
rs587779872 1.000 0.200 11 108345818 missense variant C/T snv 3.2E-05 1.4E-05 2
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs1805076 0.851 0.120 11 111764842 missense variant C/T snv 6.5E-03 7.0E-03 2
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs104894309 0.851 0.200 11 112086940 stop gained C/A;T snv 4.0E-06 4
rs80338845 0.807 0.240 11 112088971 missense variant G/T snv 7.0E-06 6