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: rs7616215
rs7616215
CCR3 ; LOC105377067
2 0.925 0.280 3 46164194 intron variant C/T snv 0.62 0.810 1.000 2 2013 2015