Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs128620185
rs128620185
BTK
4 0.882 0.240 X 101375202 missense variant C/T snv 0.010 1.000 1 1997 1997
dbSNP: rs128621195
rs128621195
BTK
2 1.000 0.120 X 101358672 missense variant T/C snv 0.010 1.000 1 1997 1997