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: rs25487
rs25487
119 0.485 0.679 19 43551574 missense variant T/C snp 0.68 0.72 0.010 1.000 1 2013 2013
dbSNP: rs746965070
rs746965070
NBN
1 1.000 0.071 8 89955487 missense variant T/C snp 1.2E-05 0.010 1.000 1 2013 2013