rs34891900, BCL2L13

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 22 17680392 intron variant C/G;T snv 0.700 1.000 1 2016 2016
Neutrophil count (procedure)
CUI: C0200633
Disease: Neutrophil count (procedure)
234 22 17680392 intron variant C/G;T snv 0.700 1.000 1 2016 2016