Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519825
BTK
X 101356176 missense variant C/G snp 1
rs1057519826
BTK
1.000 0.107 X 101356177 missense variant A/T snp 2
rs121434592 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 21
rs28904921 0.756 0.286 11 108329202 missense variant T/G snp 4.0E-05 6.4E-05 7
rs587776547 0.923 0.250 11 108331885 inframe deletion CTCTAGAATT/C in-del 2.8E-05 4
rs1057519915 0.878 0.143 1 11109318 missense variant A/C snp 4
rs1057519916 0.878 0.143 1 11109320 missense variant T/A snp 4
rs1057519913 0.923 0.107 1 11157172 missense variant G/C snp 3
rs786205165 0.878 0.107 1 11157173 missense variant C/A,T snp 4
rs1057519914 0.878 0.214 1 11157174 missense variant A/G snp 4
rs1057519854 0.923 0.107 10 121488063 missense variant A/T snp 5
rs121913476 0.846 0.107 10 121498520 missense variant A/C,T snp 5
rs1057519045 0.821 0.179 10 121498522 missense variant T/G snp 6
rs1057519901 0.923 0.107 10 121498525 missense variant T/G snp 5
rs1057519943 0.878 0.143 12 132676598 missense variant G/C,T snp 5
rs1057519944 0.878 0.143 12 132676599 missense variant G/A snp 5
rs121913348 0.801 0.214 7 140781617 missense variant C/A,G,T snp 5
rs796065354 0.801 0.107 6 151944320 missense variant A/G snp 1
rs1057519827 6 152011697 missense variant G/C snp 1
rs1057519714 6 152094402 missense variant T/C snp 1
rs1057519715 6 152098779 missense variant T/A snp 1
rs1057519716 6 152098782 missense variant C/A snp 1
rs1057519717 6 152098785 missense variant T/G snp 1
rs866987936 0.756 0.214 4 152326214 missense variant C/A,G,T snp 11
rs747241612 0.756 0.214 4 152326215 missense variant G/C snp 4.0E-06 11