rs1539019, NLRP3

N. diseases: 6
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.
Fibrinogen assay
CUI: C0337428
Disease: Fibrinogen assay
143 0.882 0.240 1 247436999 intron variant A/C snv 0.63 0.800 1.000 2 2009 2011
fibrinogen activity
CUI: C1325327
Disease: fibrinogen activity
63 0.882 0.240 1 247436999 intron variant A/C snv 0.63 0.700 1.000 2 2009 2011
Fibrinogen, CTCAE
CUI: C1561955
Disease: Fibrinogen, CTCAE
63 0.882 0.240 1 247436999 intron variant A/C snv 0.63 0.700 1.000 2 2009 2011
Anthracosis
CUI: C0003165
Disease: Anthracosis
37 0.882 0.240 1 247436999 intron variant A/C snv 0.63 0.010 1.000 1 2012 2012
Arthritis, Gouty
CUI: C0003868
Disease: Arthritis, Gouty
2356 0.882 0.240 1 247436999 intron variant A/C snv 0.63 0.010 1.000 1 2018 2018
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.882 0.240 1 247436999 intron variant A/C snv 0.63 0.010 1.000 1 2019 2019