rs12239046, NLRP3

N. diseases: 7
Source: GWASCAT ×
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.
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
250 1 247438293 intron variant T/C snv 0.58 0.800 1.000 3 2011 2019
Fibrinogen assay
CUI: C0337428
Disease: Fibrinogen assay
116 1 247438293 intron variant T/C snv 0.58 0.800 1.000 1 2011 2017
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1003 1 247438293 intron variant T/C snv 0.58 0.700 1.000 2 2016 2019
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 1 247438293 intron variant T/C snv 0.58 0.700 1.000 1 2016 2016
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1133 1 247438293 intron variant T/C snv 0.58 0.700 1.000 1 2016 2016
Granulocyte count
CUI: C0857490
Disease: Granulocyte count
150 1 247438293 intron variant T/C snv 0.58 0.700 1.000 1 2016 2016
Neutrophil count (procedure)
CUI: C0200633
Disease: Neutrophil count (procedure)
234 1 247438293 intron variant T/C snv 0.58 0.700 1.000 1 2016 2016