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: rs61754966
rs61754966
NBN
23 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.020 1.000 2 2010 2011
dbSNP: rs765602971
rs765602971
NBN
3 0.882 0.040 8 89970503 missense variant T/C snv 4.0E-06 0.010 1.000 1 2010 2010