Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs764255410 1.000 0.080 2 147918546 missense variant G/A snv 1
rs566841339 1.000 0.080 2 219489128 missense variant G/A snv 2.8E-05 2.8E-05 1
rs747576071
AXL
1.000 0.080 19 41243665 missense variant C/T snv 1.6E-05 7.0E-06 1
rs752802257 1.000 0.080 10 86923490 missense variant G/A snv 8.0E-06 7.0E-06 1
rs200035802 1.000 0.080 4 95104516 missense variant G/A snv 1.7E-04 1.5E-04 1
rs781375003 1.000 0.080 1 91964700 missense variant C/T snv 8.3E-06 7.0E-06 1
rs144130246 1.000 0.080 19 55302746 missense variant C/T snv 1.2E-05 1
rs1366698690 1.000 0.080 13 36125860 missense variant C/T snv 1
rs771803475 1.000 0.080 1 37761806 missense variant C/T snv 4.0E-06 2.8E-05 1
rs922655349 1.000 0.080 1 16131867 missense variant C/T snv 1
rs1338928289 1.000 0.080 3 135201571 missense variant G/A snv 4.0E-06 7.0E-06 1
rs762016655 1.000 0.080 7 100805514 missense variant G/A;C snv 2.2E-05; 5.5E-06 1
rs146710304 1.000 0.080 17 64054300 missense variant G/A;T snv 1.6E-05 1.4E-05 1
rs141014084 1.000 0.080 5 177430911 missense variant G/A snv 2.0E-05 2.1E-05 1
rs779372373
ITK
1.000 0.080 5 157244381 missense variant G/A snv 1.2E-05 7.0E-06 1
rs539470256 1.000 0.080 2 178779033 missense variant C/T snv 1.3E-04 7.7E-05 1
rs773256562 1.000 0.080 14 70742519 missense variant G/A snv 8.0E-06 1
rs1313508921 1.000 0.080 16 74682735 missense variant A/G snv 1.4E-05 1
rs368222977 1.000 0.080 15 88147353 missense variant G/A;C;T snv 8.4E-05; 8.0E-06 1
rs1444274116 1.000 0.080 6 117393231 missense variant A/G snv 1.4E-05 1
rs1271090915 1.000 0.080 X 20167743 missense variant T/C snv 1
rs757589345 1.000 0.080 2 219469198 missense variant G/A;C snv 4.0E-06 1
rs1331331651 1.000 0.080 17 62536325 missense variant C/A snv 8.1E-06 1
rs782203759 1.000 0.080 7 98950120 missense variant G/A snv 2.4E-05 2.8E-05 1
rs1003158162 1.000 0.080 2 178531968 missense variant G/A snv 4.0E-06 1