rs17758695, BCL2

N. diseases: 10
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 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 2 2016 2019
Finding of Mean Corpuscular Hemoglobin
1206 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 2 2016 2019
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 2 2016 2019
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 1 2016 2016
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 1 2016 2016
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 1 2016 2016
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 1 2016 2016
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 1 2016 2016
Platelet mean volume determination (procedure)
371 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 1 2016 2016
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 1 2019 2019