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: rs6003555
rs6003555
BCR
1 1.000 0.080 22 23212124 intron variant T/C snv 7.5E-02 0.700 1.000 1 2009 2009