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
rs1555114766 11 108317486 stop gained G/A snv 1
rs28904921 0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 7
rs1057519915 0.851 0.160 1 11109318 missense variant A/C snv 5
rs1057519916 0.882 0.160 1 11109320 missense variant T/A snv 4
rs1057519913 0.925 0.120 1 11157172 missense variant G/C snv 3
rs786205165 0.882 0.120 1 11157173 missense variant C/A;T snv 4
rs1057519914 0.851 0.240 1 11157174 missense variant A/G snv 4
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 2
rs1057519854 0.882 0.080 10 121488063 missense variant A/T snv 5
rs121913476 0.851 0.080 10 121498520 missense variant A/C;T snv 5
rs1057519045 0.851 0.160 10 121498522 missense variant T/G snv 6
rs1057519901 0.925 0.080 10 121498525 missense variant T/G snv 5
rs1057519943 0.790 0.160 12 132676598 missense variant G/C;T snv 5
rs1057519944 0.882 0.160 12 132676599 missense variant G/A snv 5
rs121913348 0.763 0.480 7 140781617 missense variant C/A;G;T snv 16
rs796065354 0.882 0.080 6 151944320 missense variant A/G snv 1
rs1057519827 6 152011697 missense variant G/C snv 1
rs1057519714 6 152094402 missense variant T/C snv 1
rs1057519715 1.000 0.080 6 152098779 missense variant T/A snv 1
rs1057519716 6 152098782 missense variant C/A snv 1
rs1057519717 6 152098785 missense variant T/G snv 1
rs866987936 0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs747241612 0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12