Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs128621201
BTK
0.882 0.240 X 101356060 stop gained G/A;C snv 3
rs128621193
BTK
0.925 0.120 X 101360581 stop gained G/A snv 2
rs1555977474
BTK
0.925 0.240 X 101353932 stop gained C/A;T snv 2
rs1555980049
BTK
0.925 0.120 X 101370018 stop gained C/T snv 2
rs128620187
BTK
1.000 0.120 X 101375248 stop gained G/A snv 1
rs128620188
BTK
1.000 0.120 X 101375242 stop gained G/A snv 1
rs128621191
BTK
1.000 0.120 X 101360626 stop gained C/A snv 1
rs128621192
BTK
1.000 0.120 X 101360589 stop gained C/T snv 1
rs128621199
BTK
1.000 0.120 X 101356858 stop gained G/A;T snv 1.1E-05 1
rs128621207
BTK
1.000 0.120 X 101353329 stop gained G/T snv 1
rs128622211
BTK
1.000 0.120 X 101353196 stop gained C/A snv 1
rs1555980796
BTK
1.000 0.120 X 101374612 stop gained G/T snv 1
rs1569292021
BTK
1.000 0.120 X 101357548 stop gained G/A snv 1
rs193922124
BTK
1.000 0.120 X 101356163 stop gained G/A;T snv 5.5E-06 1
rs41310709
BTK
1.000 0.120 X 101356112 stop gained G/A;T snv 1
rs128620185
BTK
0.882 0.240 X 101375202 missense variant C/T snv 4
rs1569292214
BTK
1.000 0.120 X 101358408 missense variant A/T snv 4
rs128621204
BTK
0.882 0.240 X 101353936 missense variant G/A snv 3
rs1555978277
BTK
0.882 0.240 X 101359324 missense variant C/T snv 3
rs128620183
BTK
0.925 0.120 X 101354687 missense variant C/T snv 2
rs128621194
BTK
0.925 0.240 X 101359325 missense variant G/A snv 2
rs128621195
BTK
1.000 0.120 X 101358672 missense variant T/C snv 2
rs128621202
BTK
0.925 0.240 X 101356059 missense variant C/T snv 2
rs128621203
BTK
0.925 0.240 X 101354636 missense variant A/G snv 2
rs1555980875
BTK
0.925 0.240 X 101375166 missense variant T/C snv 2