Source: ALL
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: rs1339552
rs1339552
BNC2
1 1.000 0.120 9 16848792 intron variant C/T snv 0.52 0.700 1.000 1 2009 2009