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: rs369488601
rs369488601
1 1.000 0.080 22 23181175 missense variant G/A;C snv 1.9E-05; 9.7E-05 0.010 1.000 1 2016 2016
dbSNP: rs766124888
rs766124888
BCR
1 1.000 0.080 22 23253817 missense variant C/A;G snv 4.0E-06; 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs768288452
rs768288452
1 1.000 0.080 22 23181822 missense variant A/G snv 4.1E-06 0.010 1.000 1 2012 2012
dbSNP: rs775014154
rs775014154
1 1.000 0.080 22 23181637 missense variant C/T snv 5.8E-05 7.0E-05 0.010 1.000 1 2019 2019