rs1522744, None

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 15 64895675 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 15 64895675 intron variant C/G;T snv 0.700 1.000 1 2018 2018