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: rs6437740
rs6437740
BBX
2 3 107746970 intron variant T/C snv 0.25 0.700 1.000 1 2009 2009
dbSNP: rs670752
rs670752
BBX
2 3 107594133 intron variant G/A;T snv 0.700 1.000 1 2017 2017